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Pavlovsky, & Lee Ehrman (1969). Transitional strains of Drosophila paulistorum. Evolution 23: 482–492.\nEhrman, L. (1960a). The genetics of hybrid sterility in Drosophila paulistorum. Evolution 14: 212–223.\nEhrman, L. (1965). Direct observation of sexual isolation between allopatric and between sympatric strains of the different Drosophila paulistorum races. Evolution 19: 459–464.\nHoenigsberg, H. F. & L. E. Castro (1972). Population genetics in the American Tropics. VII. The courtship behavior of Drosophila paulistorum cluster of species. (In press).\nKastritsis, C. D. (1966). A comparative chromosome study in the incipient species of the Drosophila paulistorum complex. Chromosoma 19: 208–222.\nKastritsis, C. D. (1967). A comparative study of the chromosomal polymorphs in the incipient species of the Drosophila paulistorum complex. Chromosoma 23: 180–202.\nKastritsis, C. D. (1969). A cytological study of some recently collected strains of Drosophila paulistorum. 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concerted effort to develop myriad new phenotypic alleles through mutagenesis programs presents new challenges for the biomedical community and for the informatics infrastructure needed to support this work. To handle and co-ordinate large programs of treatment, breeding, and sequential or longitudinal testing for a variety of obvious and subtle traits requires sophisticated data management software. Further, trait analyses, heritability testing, and animal availability and status must be captured and disseminated to the wider community. The Mouse Genome Database (MGD) will serve as the central integration point for the various mutagenesis programs, registering new alleles, providing accession identifiers, and capturing phenotypic descriptions. In addition, MGD will provide public access to unified searches over all alleles with links to the centres of origin for detailed testing data.",{"EN":437,"VI":438},"Visualizing the Laboratory Mouse: Capturing Phenotype Information","Trực quan hóa chuột nhắt thí nghiệm: Thu thập thông tin kiểu hình",{"VOID":440},"Ashburner, M., C. A. Ball, J. A. Blake, D. Botstein, H. Butler, J. M. Cherry, A. P. Davis, K. Dolinski, S. S. Dwight, J. T. Eppig, M. A. Harris, C. P. Hill, L. Issel-Tarver, A. Kasars-kis, S. Lewis, J. C. Matese, J. E. Richardson, M. Ringwald, G. M. Rubin & G. Sherlock, 2000. Gene Ontology: tool for the uni cation of biology. Nat. Genet. 25: 25–29.\nBlake, J. A. & M. Harris, 2003. The Gene Ontology Project: Structured vocabularies for molecular biology and their application to genome and expression analysis, in Current Protocols in Bioinformatics, edited by A. D. Baxevanis, D. B. Davison, R. Page, G. Stormo & L. Stein, Wiley & Sons, Inc., New York.\nBult, C. J., J. A. Blake, J. E. Richardson, J. A. Kadin, J. T. Eppig & the Mouse Genome Database Group, 2004. The Mouse Genome Database (MGD): integrating biology with the genome. Nucl. Acids Res. 32: D476–D481.\nDavidson, D., J. Bard, M. Kaufman & R. A. Baldock, 2001. The Mouse Atlas Database: a community resource for mouse development, Trends Genet. 17: 49–51.\nEppig, J. T., 2000. Algorithms for mutant sorting: the need for phenotype vocabularies. Mamm. Genome 11: 584–589.\nEppig, J. T. & M. Strivens, 1999. Finding a mouse: The International Mouse Strain Resource (IMSR). Trends Genet. 15: 81–82.\nPargent, W., S. Heffner, K. F. Schable, D. Soewarto, H. Fuchs & M. Hrabe de Angelis, 2000. MouseNet database: digital management of a large-scale mutagenesis project. Mamm. Genome 11: 590–593.\nRingwald, M., J. T. Eppig & J. E. Richardson, 2000. GXD: integrated access to gene expression data for the laboratory mouse. Trends Genet. 16: 188–190.\nStrivens, M. A., R. L. Selley, S. J. Greenaway, M. Hewitt, X. Liu, K. Battershill, S. L. McCormack, K. A. Pickford, L. Vizor, P. M. Nolan, A. J. Hunter, J. Peters & S. D. Brown, 2000. Informatics for mutagenesis: the design of mutabase-a distributed data recording system for animal husbandry, mutagenesis, and phenotypic analysis. Mamm. Genome 11: 577–583.",{"VOID":442},"10.1007\u002Fs10709-004-1435-7","2024-12-24T14:13:09.718+00:00",[314],"https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs10709-004-1435-7",[447,462],{"id":448,"sortIndex":19,"researcher":18,"roles":449,"affiliations":450,"properties":459,"displayName":461,"givenName":18,"familyName":18},"fe9b0883-710a-400f-92c3-be4c2909136f",[320],[451],{"id":452,"sortIndex":19,"affiliation":453,"properties":18},"210509a5-ed73-4d2a-a329-4f00abc89000",{"id":452,"createTime":18,"updateTime":18,"relativeEntities":454,"slug":18,"properties":455,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":458,"statistic":18},[],{"title":456},{"VI":457},"Informatics Group, Mammalian Genetics Unit & UK Mouse Genome Centre, UK",[],{"title":460},{"VI":461},"Mark Strivens",{"id":463,"sortIndex":222,"researcher":18,"roles":464,"affiliations":465,"properties":483,"displayName":485,"givenName":18,"familyName":18},"b2b20a07-528e-4883-b928-36e91d03382f",[320],[466,474],{"id":467,"sortIndex":19,"affiliation":468,"properties":18},"c6373ce7-97c8-41de-98a6-7101468c16f1",{"id":467,"createTime":18,"updateTime":18,"relativeEntities":469,"slug":18,"properties":470,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":473,"statistic":18},[],{"title":471},{"VI":472},"The Jackson Laboratory, USA",[],{"id":475,"sortIndex":222,"affiliation":476,"properties":482},"71778a21-66e7-473a-9be5-86ce7d55fe1c",{"id":475,"createTime":18,"updateTime":18,"relativeEntities":477,"slug":18,"properties":478,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":481,"statistic":18},[],{"title":479},{"VI":480},"Lexicon Genetics, Inc., USA",[],{},{"title":484},{"VI":485},"Janan T. Eppig",{"url":445,"publisher":487,"properties":544},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":488,"slug":10,"properties":489,"entityType":16,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":19,"subjectFields":492,"manageAffiliations":513,"indexDatabases":524,"url":18,"thumbnailPath":18,"statistic":539,"gsStatistic":18,"type":18,"analyzePriority":18},[],{"issn":490,"title":491},{"VOID":13},{"EN":15},[493,497,501,505,509],{"id":22,"createTime":18,"updateTime":18,"relativeEntities":494,"label":495,"description":496,"parentId":18,"standard":18,"scholarHubFieldId":18},[],{"EN":25},{},{"id":28,"createTime":18,"updateTime":18,"relativeEntities":498,"label":499,"description":500,"parentId":18,"standard":18,"scholarHubFieldId":18},[],{"EN":31},{},{"id":34,"createTime":18,"updateTime":18,"relativeEntities":502,"label":503,"description":504,"parentId":18,"standard":18,"scholarHubFieldId":18},[],{"EN":37},{},{"id":40,"createTime":18,"updateTime":18,"relativeEntities":506,"label":507,"description":508,"parentId":18,"standard":18,"scholarHubFieldId":18},[],{"EN":43},{},{"id":46,"createTime":18,"updateTime":18,"relativeEntities":510,"label":511,"description":512,"parentId":18,"standard":18,"scholarHubFieldId":18},[],{"EN":49},{},[514,519],{"id":53,"createTime":18,"updateTime":18,"relativeEntities":515,"slug":18,"properties":516,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":518,"statistic":18},[],{"title":517},{"EN":57},[],{"id":60,"createTime":18,"updateTime":18,"relativeEntities":520,"slug":18,"properties":521,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":523,"statistic":18},[],{"title":522},{"EN":64},[66],[525,532],{"id":69,"indexDatabase":526,"url":80,"indexYears":81,"academicFieldIds":531,"indexDatabaseRanking":88},{"id":71,"createTime":18,"updateTime":18,"relativeEntities":527,"label":528,"description":529,"key":77,"publicationTags":530,"standard":18},[],{"EN":74,"VI":74},{"EN":74,"VI":76},[79],[83,84,85,86,87],{"id":90,"indexDatabase":533,"url":103,"indexYears":18,"academicFieldIds":538,"indexDatabaseRanking":18},{"id":92,"createTime":18,"updateTime":18,"relativeEntities":534,"label":535,"description":536,"key":99,"publicationTags":537,"standard":18},[],{"EN":95,"VI":95},{"EN":97,"VI":98},[101,102],[105],{"impactFactor":19,"impactFactorByYear":540,"i10Index":119,"i10IndexLast5Year":19,"totalPublication":120,"totalPublicationByYear":541,"totalCitation":183,"totalCitationByYear":542,"totalCitationPerPublication":223,"totalCitationPerPublicationByYear":543,"hindexLast5Year":141,"hindex":141},{"2012":108,"2013":109,"2014":110,"2015":110,"2016":111,"2017":112,"2018":113,"2019":114,"2020":115,"2021":116,"2022":117,"2023":118},{"1919":122,"1920":123,"1921":124,"1922":125,"1923":126,"1924":127,"1925":128,"1926":129,"1927":130,"1928":131,"1929":132,"1930":126,"1931":133,"1932":134,"1933":135,"1934":126,"1935":136,"1936":122,"1937":137,"1938":129,"1939":135,"1940":132,"1941":131,"1943":138,"1949":124,"1951":124,"1953":135,"1955":128,"1957":122,"1959":139,"1960":140,"1962":129,"1963":136,"1964":141,"1965":123,"1966":142,"1967":143,"1968":144,"1969":145,"1970":146,"1971":147,"1972":148,"1973":149,"1974":127,"1975":150,"1976":151,"1977":136,"1978":152,"1979":153,"1980":154,"1981":155,"1982":156,"1983":157,"1984":158,"1985":159,"1986":160,"1987":155,"1988":161,"1989":136,"1990":162,"1991":156,"1992":163,"1993":164,"1994":165,"1995":166,"1996":167,"1997":155,"1998":168,"1999":169,"2000":170,"2001":171,"2002":170,"2003":172,"2004":173,"2005":164,"2006":174,"2007":175,"2008":176,"2009":177,"2010":178,"2011":160,"2012":179,"2013":179,"2014":180,"2015":181,"2016":168,"2017":152,"2018":146,"2019":142,"2020":135,"2021":144,"2022":147,"2023":128,"2024":182},{"1920":131,"1921":138,"1922":185,"1923":148,"1924":140,"1925":150,"1926":131,"1927":186,"1928":127,"1929":185,"1930":170,"1931":171,"1932":182,"1933":139,"1935":122,"1936":131,"1937":124,"1938":131,"1939":187,"1940":133,"1941":188,"1949":185,"1953":189,"1955":190,"1959":191,"1963":147,"1964":158,"1966":168,"1967":192,"1969":193,"1970":194,"1971":127,"1972":181,"1973":149,"1974":140,"1975":155,"1976":191,"1977":195,"1978":196,"1979":195,"1980":197,"1981":198,"1982":199,"1983":200,"1984":178,"1985":168,"1986":201,"1987":202,"1988":203,"1989":168,"1990":204,"1991":205,"1992":206,"1993":207,"1994":208,"1995":209,"1996":210,"1997":211,"2003":176,"2004":212,"2005":213,"2006":214,"2007":215,"2008":210,"2009":216,"2010":217,"2011":218,"2012":154,"2013":219,"2014":162,"2015":220,"2016":221,"2017":191,"2018":177,"2019":148,"2020":138,"2021":126,"2022":140,"2023":185,"2024":222},{"1920":115,"1921":225,"1922":226,"1923":227,"1924":228,"1925":229,"1926":230,"1927":231,"1928":232,"1929":233,"1930":234,"1931":235,"1932":236,"1933":237,"1935":238,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zipper (HD-Zip) transcription factors regulate developmental processes and stress responses in plants, and they vary widely in gene number and family structure. In this study, 55 predicted maize HD-Zip genes were systematically analyzed with respect to their phylogenetic relationships, molecular evolution, and gene expression in order to understand the functional diversification within the family. Phylogenetic analysis of HD-Zip proteins from Zea mays, Oryza sativa, Arabidopsis thaliana, Vitis vinifera, and Physcomitrella patens showed that they group into four classes. We inferred that the copy numbers of classes I and III genes were relatively conserved in all five species. The 55 maize HD-Zip genes are distributed randomly on the ten chromosomes, with 15 segmental duplication and 4 tandem duplication events, suggesting that segmental duplications were the major contributors in the expansion of the maize HD-Zip gene family. Expression analysis of the 55 maize HD-Zip genes in different tissues and drought conditions revealed differences in the expression levels and patterns between the four classes. Promoter analysis revealed that a number of stress response-, hormone response-, light response-, and development-related cis-acting elements were present in their promoters. Our results provide novel insights into the molecular evolution and gene expression within the HD-Zip gene family in maize, and provide a solid foundation for future functional study of the HD-Zip genes in maize.",{"EN":562,"VI":563},"Molecular evolution and gene expression differences within the HD-Zip transcription factor family of Zea mays L.","Tiến hóa phân tử và những khác biệt về biểu hiện gene trong họ yếu tố phiên mã HD-Zip của Zea mays L.",{"VOID":565},"Aoyama T, Dong CH, Wu Y, Carabelli M, Sessa G, Ruberti I, Morelli G, Chua NH (1995) Ectopic expression of the Arabidopsis transcriptional activator Athb-1 alters leaf cell fate in tobacco. Plant Cell 7:1773–1785\nArce AL, Raineri J, Capella M, Cabello JV, Chan RL (2011) Uncharacterized conserved motifs outside the HD-Zip domain in HD-Zip subfamily I transcription factors; a potential source of functional diversity. BMC Plant Biol 11:42\nAriel FD, Manavella PA, Dezar CA, Chan RL (2007) The true story of the HD-Zip family. Trends Plant Sci 12:419–426\nBadis G, Berger MF, Philippakis AA, Talukder S, Gehrke AR, Jaeger SA, Chan ET, Metzler G, Vedenko A, Chen X, Kuznetsov H, Wang CF, Coburn D, Newburger DE, Morris Q, Hughes TR, Bulyk ML (2009) Diversity and complexity in DNA recognition by transcription factors. Science 324:1720–1723\nBaima S, Possenti M, Matteucci A, Wisman E, Altamura MM, Ruberti I, Morelli G (2001) The Arabidopsis ATHB-8 HD-Zip protein acts as a differentiation-promoting transcription factor of the vascular meristems. Plant Physiol 126:643–655\nBanks JA, Nishiyama T, Hasebe M, Bowman JL, Gribskov M, dePamphilis C, Albert VA, Aono N, Aoyama T (2011) The Selaginella genome identifies genetic changes associated with the evolution of vascular plants. Science 332:960–963\nBlanc G, Wolfe KH (2004) Functional divergence of duplicated genes formed by polyploidy during Arabidopsis evolution. Plant Cell 16:1679–1691\nBowers JE, Chapman BA, Rong J, Paterson AH (2003) Unravelling angiosperm genome evolution by phylogenetic analysis of chromosomal duplication events. Nature 422:433–438\nBowman JL, Floyd SK, Sakakibara K (2007) Green genes-comparative genomics of the green branch of life. Cell 129:229–234\nCannon SB, Mitra A, Baumgarten A, Young ND, May G (2004) The roles of segmental and tandem gene duplication in the evolution of large gene families in Arabidopsis thaliana. BMC Plant Biol 4:10\nCarabelli M, Sessa G, Baima S, Morelli G, Ruberti I (1993) The Arabidopsis Athb-2 and -4 genes are strongly induced by far-red-rich light. Plant J 4:469–479\nChen X, Chen Z, Zhao H, Zhao Y, Cheng B, Xiang Y (2014) Genome-wide analysis of soybean HD-Zip gene family and expression profiling under salinity and drought treatments. PLoS ONE 9:e87156\nChenna R, Sugawara H, Koike T, Lopez R, Gibson TJ, Higgins DG, Thompson JD (2003) Multiple sequence alignment with the Clustal series of programs. Nucleic Acids Res 31:3497–3500\nDi Cristina M, Sessa G, Dolan L, Linstead P, Baima S, Ruberti I, Morelli G (1996) The Arabidopsis Athb-10 (GLABRA2) is an HD-Zip protein required for regulation of root hair development. Plant J 10:393–402\nEmery JF, Floyd SK, Alvarez J, Eshed Y, Hawker NP, Izhaki A, Baum SF, Bowman JL (2003) Radial patterning of Arabidopsis shoots by class III HD-ZIP and KANADI genes. Curr Biol 13:1768–1774\nFinn RD, Mistry J, Schuster-Böckler B, Griffiths-Jones S, Hollich V, Lassmann T, Moxon S, Marshall M, Khanna A, Durbin R, Eddy SR, Sonnhammer EL, Bateman A (2014) Pfam: clans, web tools and services. Nucleic Acids Res 34:D247–D251\nGaut BS, Morton BR, McCaig BC, Clegg MT (1996) Substitution rate comparisons between grasses and palms: synonymous rate differences at the nuclear gene Adh parallel rate differences at the plastid gene rbcL. Proc Natl Acad Sci USA 93:10274–10279\nGu Z, Steinmetz LM, Gu X, Scharfe C, Davis RW, Li WH (2003) Role of duplicate genes in genetic robustness against null mutations. Nature 421:63–66\nGuo AY, Zhu QH, Chen X, Luo JC (2007) GSDS: a gene structure display server. Yi Chuan 29:1023–1026\nHanada K, Zou C, Lehti-Shiu MD, Shinozaki K, Shiu SH (2008) Importance of lineage-specific expansion of plant tandem duplicates in the adaptive response to environmental stimuli. Plant Physiol 148:993–1003\nHarris JC, Hrmova M, Lopato S, Langridge P (2011) Modulation of plant growth by HD-Zip class I and II transcription factors in response to environmental stimuli. New Phytol 190:823–837\nHimmelbach A, Hoffmann T, Leube M, Höhener B, Grill E (2002) Homeodomain protein ATHB6 is a target of the protein phosphatase ABI1 and regulates hormone responses in Arabidopsis. EMBO J 21:3029–3038\nHobert O (2008) Gene regulation by transcription factors and microRNAs. Science 319:1785–1786\nHu R, Chi X, Chai G, Kong Y, He G, Wang X, Shi D, Zhang D, Zhou G (2012) Genome-wide identification, evolutionary expansion, and expression profile of homeodomain-leucine zipper gene family in poplar (Populus trichocarpa). PLoS ONE 7:e31149\nHuang D, Wu W, Abrams SR, Cutler AJ (2008) The relationship of drought-related gene expression in Arabidopsis thaliana to hormonal and environmental factors. J Exp Bot 59:2991–3007\nJin J, Zhang H, Kong L, Gao G, Luo J (2014) PlantTFDB 3.0: a portal for the functional and evolutionary study of plant transcription factors. Nucleic Acids Res 42:D1182–D1187\nJohannesson H, Wang Y, Hanson J, Engström P (2003) The Arabidopsis thaliana homeobox gene ATHB5 is a potential regulator of abscisic acid responsiveness in developing seedlings. Plant Mol Biol 51:719–729\nJuretic N, Hoen DR, Huynh ML, Harrison PM, Bureau TE (2005) The evolutionary fate of MULE-mediated duplications of host gene fragments in rice. Genome Res 15:1292–1297\nKong H, Landherr LL, Frohlich MW, Leebens-Mack J, Ma H, dePamphilis CW (2007) Patterns of gene duplication in the plant SKP1 gene family in angiosperms: evidence for multiple mechanisms of rapid gene birth. Plant J 50:873–885\nLetunic I, Copley RR, Schmidt S, Ciccarelli FD, Doerks T, Schultz J, Ponting CP, Bork P (2004) SMART 4.0: towards genomic data integration. Nucleic Acids Res 32:D142–D144\nLi WH, Yang J, Gu X (2005) Expression divergence between duplicate genes. Trends Genet 21:602–607\nLiu Y, Zhang D, Wang L, Li D (2013) Genome-wide analysis of mitogen-activated protein kinase gene family in maize. Plant Mol Biol Rep 31:1446–1460\nLivak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods 25:402–408\nLynch M, Conery JS (2000) The evolutionary fate and consequences of duplicate genes. Science 290:1151–1155\nMao H, Wang H, Liu S, Li Z, Yang X, Yan J, Li J, Tran LS, Qin F (2015) A transposable element in a NAC gene is associated with drought tolerance in maize seedlings. Nat Commun 6:8326\nNakamura M, Katsumata H, Abe M, Yabe N, Komeda Y, Yamamoto KT, Takahashi T (2006) Characterization of the class IV homeodomain-Leucine Zipper gene family in Arabidopsis. Plant Physiol 141:136–1375\nOhashi-Ito K, Fukuda H (2003) HD-Zip III homeobox genes that include a novel member, ZeHB-13 (Zinnia)\u002FATHB-15 (Arabidopsis), are involved in procambium and xylem cell differentiation. Plant Cell Physiol 44:1350–1358\nOlsson AS, Engström P, Söderman E (2004) The homeobox genes ATHB12 and ATHB7 encode potential regulators of growth in response to water deficit in Arabidopsis. Plant Mol Biol 55:663–677\nPeng X, Zhao Y, Cao J, Zhang W, Jiang H, Li X, Ma Q, Zhu S, Cheng B (2012) CCCH-type zinc finger family in maize: genome-wide identification, classification and expression profiling under abscisic acid and drought treatments. PLoS ONE 7:e40120\nRensing SA, Lang D, Zimmer AD, Terry A, Salamov A, Shapiro H, Nishiyama T, Perroud PF, Lindquist EA (2008) The Physcomitrella genome reveals evolutionary insights into the conquest of land by plants. Science 319:64–69\nRerie WG, Feldmann KA, Marks MD (1994) The GLABRA2 gene encodes a homeo domain protein required for normal trichome development in Arabidopsis. Genes Dev 8:1388–1399\nRicachenevsky FK, Sperotto RA, Menguer PK, Fett JP (2010) Identification of Fe-excess-induced genes in rice shoots reveals a WRKY transcription factor responsive to Fe, drought and senescence. Mol Biol Rep 37:3735–3745\nSawa S, Ohgishi M, Goda H, Higuchi K, Shimada Y, Yoshida S, Koshiba T (2002) The HAT2 gene, a member of the HD-Zip gene family, isolated as an auxin inducible gene by DNA microarray screening, affects auxin response in Arabidopsis. Plant J 32:1011–1022\nSchena M, Davis RW (1994) Structure of homeobox-leucine zipper genes suggests a model for the evolution of gene families. 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Development 126:4235–4245\nTamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28:2731–2739\nVan Camp W (2005) Yield enhancement genes: seeds for growth. Curr Opin Biotech 16:147–153\nWalford SA, Wu Y, Llewellyn DJ, Dennis ES (2011) GhMYB25-like: a key factor in early cotton fibre development. Plant J 65:785–797\nWang Y, Henriksson E, Söderman E, Henriksson KN, Sundberg E, Engström P (2003) The Arabidopsis homeobox gene, ATHB16, regulates leaf development and the sensitivity to photoperiod in Arabidopsis. Dev Biol 264:228–239\nYang ZH (2007) PAML 4: phylogenetic analysis by maximum likelihood. Mol Biol Evol 24:1586–1591\nZhao Y, Zhou Y, Jiang H, Li X, Gan D, Peng X, Zhu S, Cheng B (2011) Systematic analysis of sequences and expression patterns of drought-responsive members of the HD-Zip gene family in maize. 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Biol. 16: 175?197.",{"doi":1179},"10.1101\u002FSQB.1951.016.01.015",{"id":18,"text":1181,"url":18,"identifiers":1182},"Suzuki, D. T. (1962). Interchromosomal effects on crossing over in Drosophila melanogaster. I. Effects of compound and ring X chromosomes on the third chromosomes. Genetics 47: 305?319 ? (1964). Corrigenda Genetics 50: 1453.",{"doi":1183},"10.1093\u002Fgenetics\u002F47.3.305",{"id":18,"text":1185,"url":18,"identifiers":1186},"Williamson, J. H. (1966). Interchromosomal effects of autosomal translocations on recombination in Drosophila melanogaster. Genetics 54: 1431?1440.",{"doi":1187},"10.1093\u002Fgenetics\u002F54.6.1431",{"id":1189,"createTime":1190,"updateTime":1191,"relativeEntities":1192,"slug":1193,"properties":1194,"entityType":309,"verifyStatus":310,"verifyTime":1205,"verifyNote":312,"languages":18,"translateLanguages":18,"viewCount":19,"primaryUrl":1206,"fullTextUrl":18,"authors":1207,"publicationType":359,"publisherRelationship":1225,"citationCount":19,"citationInfo":1288,"publishDate":1291,"publishYear":1289,"citationAnalyzeStatus":17,"lastCitationAnalyze":1292,"indexDatabases":1293,"openAccess":18,"references":18,"isForceReanalyzing":426},"60fc4e02-e267-48fc-808f-636dd09a2294","2023-12-12T15:22:05.724+00:00","2026-07-21T13:00:06.810+00:00",[],"Nucleo-cytoplasmic-interactions-causing-partial-female-sterility-in-the-spider-mite-Tetranychus-urticae-Koch-Acari-Tetranychidae-",{"abstract":1195,"title":1197,"gsPaper":1199,"references":1201,"doi":1203},{"EN":1196},"A case of non-reciprocal hybrid infertility between strains of the spider mite Tetranychus urticae Koch is described. Evidence is presented that the infertility results from an interaction between a chromosomal and a cytoplasmic factor. The presence or absence of the cytoplasmic factor seems to be controlled also by chromosomal genes.",{"EN":1198},"Nucleo-cytoplasmic interactions causing partial female sterility in the spider mite Tetranychus urticae Koch (Acari: Tetranychidae)",{"VOID":1200},"[\"4337810393936415857\"]",{"VOID":1202},"Boudreaux, H. B., 1963. Biological aspects of some phytophagous mites. A. Rev. Ent. 8: 137–154.\nBucheton, A., 1978. Non-Mendelian female sterility in Drosophila melanogaster: influence of ageing and thermic treatments I. Evidence for a partly inheritable effect of these two factors. Heredity 41: 357–369.\nBucheton, A., 1979 a. Non-Mendelian female sterility in Drosophila melanogaster: Influence of ageing and thermic treatments II. Biol. cellulaire 34: 43–50.\nBucheton, A., 1979 b. Non-Mendelian female sterility in Drosophila melanogaster: Influence of ageing and thermic treatments III. Genetics 93: 131–142.\nBucheton, A. & Picard, G., 1978. Non-Mendelian female sterility in Drosophila melanogaster: Hereditary transmission of reactivity levels. Heredity 40: 207–223.\nDeBoer, R., 1980. Genetic affinities between spider mite Tetranychus urticae populations in a non-agricultural area. Ent. exp. & appl. 28: 22–28.\nDeBoer, R., 1981. Genetic affinities between spider mite Tetranychus urticae populations in a non-agricultural area II. Ent. exp. & appl. 30: 63–67.\nDillon, L. S., 1958. Reproductive isolation among certain spider mites of the Tetranychus telarius complex, with preliminary systematic notes. Ann. ent. Soc. Am. 51: 441–448.\nDosse, G. & Langenscheidt, M., 1964. Morphologische, biologische und histologische Untersuchungen an Hybriden aus dem Tetranychus urticae cinnabarinus-Komplex. Z. angew. Ent. 54: 349–359.\nEngels, W. R. & Preston, C. R., 1980. Components of hybrid dysgenesis in a wild population of Drosophila melanogaster. Genetics 95: 111–128.\nHelle, W., 1962. Genetics of resistance to organophosphorous compounds and its relation to diapause. Tijdschr. Pl Ziekt. 68: 155–195.\nKearsey, M. J., Williams, W. R., Allen, P. & Coulter, F., 1977. Polymorphism for chromosomes capable of inducing female sterility in Drosophila. Heredity 38: 109–115.\nKidwell, M. G., 1979. Hybrid dysgenesis in Drosophila melanogaster: the relationship between the P-M and I-R systems. Genet. Res. 33: 205–217.\nKidwell, M. G., Kidwell, J. F. & Sved, J. A., 1977. Hybrid dysgenesis in Drosophila melanogaster: A syndrome of aberrant traits including mutation, sterility and male recombination. Genetics 86: 813–833.\nKeh, B., 1952. Mating experiments with the two-spotted spider mite complex. J. econ. Ent. 45: 308–312.\nOvermeer, W. P. J. & Zon, A. Q.van, 1976. Partial reproductive incompatibility between populations of spider mites. Ent. exp. & appl. 20: 225–236.\nPélisson, A., 1978. Non-Mendelian female sterility in Drosophila melanogaster: variations of chromosomal contamination when caused by chromosomes of various inducer efficiencies. Genet. Res. 32: 113–122.\nPélisson, A. & Picard, G., 1979. Non-Mendelian female sterility in Drosophila melanogaster: I-factor mapping on inducer chromosomes. Genetica 50: 141–148.\nPicard, G., 1976. Non-Mendelian female sterility in Drosophila melanogaster: Hereditary transmission of I-factor. Genetics 83: 107–123.\nPicard, G., 1978 a. Non-Mendelian female sterility in Drosophila melanogaster: sterility in the daughter progeny of SF and RSF females. Biol. Cellulaire 31: 235–244.\nPicard, G., 1978 b. Non-Mendelian female sterility in Drosophila melanogaster: sterility in stocks derived from the genotypically inducer or reactive offspring of SF and RSF females. Biol. cellulaire 31: 245–254.\nPicard, G., 1978 c. Non-Mendelian female sterility in Drosophila melanogaster, further data on chromosomal contamination. Molec. gen. Genet. 164: 235–247.\nPicard, G., 1979. Non-Mendelian female sterility in Drosophila melanogaster: principal characteristics of chromosomes from inducer and reactive origin after chromosomal contamination. Genetics 91: 455–471.\nPicard, G., Bucheton, A., Lavige, J. M. & Pélisson, A., 1976. Répartition géographique des trois types de souches impliquées dans un phénomène de stérilité à déterminisme non mendélien chez Drosophila melanogaster. C. R. Acad. Sc. Paris D 282: 1813–1816.",{"VOID":1204},"10.1007\u002FBF00055998","2024-05-10T07:07:30.508+00:00","http:\u002F\u002Flink.springer.com\u002F10.1007\u002FBF00055998",[1208],{"id":1209,"sortIndex":19,"researcher":18,"roles":1210,"affiliations":1211,"properties":1220,"displayName":1222,"givenName":18,"familyName":18},"44ba014c-6668-4828-9ce6-7ca7db3431d4",[320],[1212],{"id":1213,"sortIndex":19,"affiliation":1214,"properties":18},"14bd5601-98a1-4c10-a37d-7063f4f6b16c",{"id":1213,"createTime":18,"updateTime":18,"relativeEntities":1215,"slug":18,"properties":1216,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":1219,"statistic":18},[],{"title":1217},{"VI":1218},"Laboratory of Experimental Entomology, University of Amsterdam, Amsterdam, The Netherlands",[],{"title":1221,"gsAuthor":1223},{"VI":1222},"R. 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class of repetitive DNA sequences frequently found at centromeric regions are R\u002FY-satellites showing an asymmetric distribution of residues resulting in one strand being rich in purines (R-strand) while the complementary strand is pyrimidine-rich (Y-strand). The dodeca-satellite of Drosophila belongs to this class of centromeric satellites. In vitro, the dodeca-satellite forms altered DNA structures in which the R-strand forms very stable intramolecular fold-backs that are stabilised by the formation of tandem G · A mismatches. A single-stranded nucleic acids binding protein, DDP1, binds the unstructured dodeca-satellite Y-strand with high affinity. In polytene chromosomes, DDP1 associates with the heterochromatic chromocenter and, at the euchromatic chromosome arms, co-localises with HP1. DDP1 is a vigilin. Vigilins are highly conserved multi-KH-domain proteins. Scp160p, the vigilin from S. cerevisiae, is involved in the control of ploidy. 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A. B. D., 1934, A remarkable cross in Mus musculus, Genetica, 16 p. 321–359.","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF02071501",{"doi":1697},"10.1007\u002FBF02071501",{"id":1699,"text":1700,"url":1701,"identifiers":1702},"65ee4932-b498-465f-95b0-46c6a3a0b120","Fortuyn, A. B. D., 1935, The influence of the sex chromosome on the number of tailrings in Mus musculus, Genetica, 17 p. 291–298.","http:\u002F\u002Flink.springer.com\u002F10.1007\u002FBF01985015",{"doi":1703},"10.1007\u002FBF01985015",{"id":856,"text":1705,"url":858,"identifiers":1706},"Fortuyn, A. B. D., 1939, A polydactylous strain of mice. Genetica 21 p. 97.",{"doi":860},{"id":18,"text":1708,"url":18,"identifiers":1709},"Green, C. V., 1933, Inheritance of foot length in a mouse species cross, Journal of Heredity, 24 p. 440–442.",{},{"id":1711,"createTime":1712,"updateTime":1713,"relativeEntities":1714,"slug":1715,"properties":1716,"entityType":309,"verifyStatus":310,"verifyTime":1727,"verifyNote":312,"languages":18,"translateLanguages":18,"viewCount":19,"primaryUrl":1728,"fullTextUrl":18,"authors":1729,"publicationType":359,"publisherRelationship":1786,"citationCount":131,"citationInfo":1849,"publishDate":1852,"publishYear":1850,"citationAnalyzeStatus":845,"lastCitationAnalyze":1853,"indexDatabases":1854,"openAccess":18,"references":18,"isForceReanalyzing":426},"b2c109e9-fed0-466a-8124-78d98c93264f","2024-01-12T20:42:10.222+00:00","2026-07-18T01:09:04.994+00:00",[],"Nucleotide-sequence-analysis-of-a-mouse-Y-chromosomal-DNA-fragment-containing-Bkm-and-LINE-elements",{"abstract":1717,"title":1719,"gsPaper":1721,"references":1723,"doi":1725},{"EN":1718},"The strong suppression of crossing-over between the X and Y chromosomes permits rapid accumulation of repetitive sequences in the Y chromosome. To gain insight into the mechanism responsible for the sequence amplification, it is essential to characterize Y chromosomal repetitive sequences at the molecular level. Here, we report the entire nucleotide sequence (3,902bp) of AC11, a mouse sequence that is repeated 300 times in the Y chromosome. AC11 is AT rich (32.8% GC), and contains many short poly(A) sequences. In addition, it has Bkm and LINE sequences as well as a Y chromosome-specific sequence. The Bkm sequence consists of typical (GATA) and (GACA) repeating units, whereas the LINE sequence deviates considerably from other mouse LINE sequences (71–76% identity) and may be considered atypical. The Y chromosome-specific region seems to be unique and does not identify similar sequences in the GenBank library. The information obtained from the nucleotide sequence should form the foundation to study the evolutionary processes through which AC11-related sequences have accumulated in the mouse Y chromosome.",{"EN":1720},"Nucleotide sequence analysis of a mouse Y chromosomal DNA fragment containing Bkm and LINE elements",{"VOID":1722},"[\"12859727215837406344\"]",{"VOID":1724},"Biddle, F.G., B.A., Eales & Y., Nishioka, 1991. A DNA polymorphism from five inbred strains of the mouse identifies a functional class of domesticus Y chromosome that produces the same phenotypic distribution of gonadal hermaphrodites. Genome 34: 96–104.\nBiddle, F.G. & Y., Nishioka, 1988. Assays of testis development in the mouse distinguish three classes of domesticus-type Y chromosome. Genome 30: 870–878.\nBishop, C.E., P., Boursot, B., Barron, F., Bonhomme & D., Hatat, 1985. Most classical Mus musculus domesticus laboratory mouse strains carry a Mus musculus musculus Y chromosome. Nature 315: 70–72.\nCharlesworth, B., 1991. The evolution of sex chromosomes. Science 251: 1030–1033.\nDubnick, M., J., Chou, T.D., Peter & R.A., Farber, 1983. Relationships among DNA sequences of the 1.3 kb EcoRI family of mouse DNA. J. Mol. Evol. 19: 115–121.\nEicher, E.M., K.W., Hutchison, S.J., Phillips, P.K., Tucker & B., Lee, 1989. A repeated segment on the mouse Y chromosome is composed of retroviral-related, Y-enriched and Y-specific sequences. Genetics 122: 181–192.\nEpplen, J.T., A., Cellini, S., Romero & S., Ohno, 1983. An attempt to approach the molecular mechanisms of primary sex determination. W- and Y-chromosomal conserved simple repetitive DNA sequences and their differential expression in mRNA. J. Exp. Zool. 228: 305–312.\nEpplen, J.T., J.R., McCarrey, S., Sutou & S., Ohno, 1982. Base sequence of a cloned snake. W-chromosome DNA fragment and identification of a male-specific putative mRNA in the mouse. Proc. Natl. Acad. Sci. U.S.A. 79: 3798–3802.\nFanning, T.G., 1983. Size and structure of a highly repetitive BAM HI element in mice. Nuc. Acids Res. 11: 5073–5091.\nJones, K.W. & L., Singh, 1981. Conserved repeated DNA sequences in vertebrate sex chromosomes. Human Genet. 58: 46–53.\nKrayev, A.S., D.A., Kramerov, K.G., Skryabin, A.P., Ryskov, A.A., Bayer & G.P., Georgiev, 1980. The nucleotide sequence of the ubiquitous repetitive DNA sequence B1 complementary to the most abundant class of mouse fold-back RNA. Nuc. Acids Res. 8: 1201–1215.\nLamar, E.E. & E., Palmer, 1984. Y-enriched, species-specific DNA in mice: Evidence that the Y chromosome exists in two polymorphic forms in inbred strains. Cell 37: 171–177.\nLoeb, D.D., R.W., Padgett, S.C., Hardies, W.R., Shehee, M.B., Comer, M.H., Edgell & C.A., Hutchison, 1986. The sequence of a large L1Md element reveals a tandemly repeated 5′ end and several features found in retrotransposons. Mol. Cell. Biol. 6: 168–182.\nMeunier-Rotival, M. & G., Bernardi, 1984. The Bam repeats of the mouse genome belong in several superfamilies the longest of which is over 9 kb in size. Nuc. Acids Res. 12: 1593–1608.\nNallaseth, F.-S. & M.J., Dewey, 1986. Moderately repeated mouse Y chromosomal sequence families present distinct types of organization and evolutionary change. Nuc. Acids Res. 14: 5295–5307.\nNallaseth, F.-S., R.P., Lawther, M.R., Stallup & M.J., Dewey, 1983. Isolation of recombinant bacteriophage containing male specific mouse DNA. Mol. Gen. Genet. 190: 80–84.\nNishioka, Y., 1987. Y-chromosomal DNA polymorphism in mouse inbred strains. Genet. Res. 50: 69–72.\nNishioka, Y., 1988a. Application of Y chromosomal repetitive sequences to sexing mouse embryos. Teratology 38: 181–185.\nNishioka, Y., 1988b. Evolutionary characterization of a Y chromosomal sequence conserved in the genus Mus. Genet. Res. 52: 145–150.\nNishioka, Y., 1989. Genome comparison in the genus Mus: a study with B1, MIF (mouse interspersed fragment), centromeric and Y-chromosomal repetitive sequences. Cytogent: Cell Genet. 50: 195–200.\nNishioka, Y. & E., Lamothe, 1986. Isolation and characterizatio of a mouse Y chromosomal repetitive sequence. Genetics 113: 417–432.\nNishioka, Y. & E., Lamothe, 1987a. Evolution of a mouse Y chromosomal sequence flanked by highly repetitive elements. Genome 29: 380–383.\nNishioka, Y. & E., Lamothe, 1987b. The Mus musculus musculus type Y chromosome predominates in Asian house mice. Genet. Res. 50: 195–198.\nSanger, F., S., Nicklen & A.R., Coulson, 1977. DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. U.S.A. 74: 5463–5467.\nSchäfer, R., E., Böltz, A., Becker, F., Bartlets & J.T., Epplen, 1986. The expression of the evolutionarily conserved GATA\u002FGACA repeats in mouse tissues. Chromosoma 93: 496–501.\nSinger, M.F., 1982. Highly repeated sequences in mammalian genomes. Int. Rev.Cytol. 76: 67–112.\nSingh, L. & K., Jones, 1982. Sex reversal in the mouse (Mus musculus) is caused by a recurrent nonreciprocal crossover involving the X and an aberrant Y chromosome. Cell 28: 205–216.\nSingh, L., C., Phillips & K.W., Jones, 1984. The conserved nucleotide sequences of Bkm, which define Sxr in the mouse, are transcribed. Cell 36: 111–120.\nSingh, L., I.F., Purdom & K.W., Jones, 1980. Sex chromosome associated satellite DNA: evolution and conservation. Chromosoma 79: 137–157.\nTaketo-Hosotani, T., Y., Nishioka, C.M., Nagamine, I., Villalpando & H., Merchant-Larios, 1989. Development and fertility of ovaries in the B6.YDOM sex-reversed female mouse. Development 107: 95–105.\nTucker, P.K., B.K., Lee & E.M., Eicher, 1989. Y chromosome evolution in the subgenus Mus (genus Mus). Genetics 122: 169–179.\nVoliva, C.F., C.L., Jahn, M.B., Comer, M.H., Edgell & C.A., Hutchison, 1983. The L1Md long interspersed repeat family in the mouse: almost all examples are truncated at one end. Nucl. Acids Res. 11: 8847–8859.",{"VOID":1726},"10.1007\u002FBF00128768","2024-05-27T19:33:02.985+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF00128768",[1730,1745,1758,1771],{"id":1731,"sortIndex":19,"researcher":18,"roles":1732,"affiliations":1733,"properties":1742,"displayName":1744,"givenName":18,"familyName":18},"fdb5802f-1067-4f0f-be90-81702cca2d0c",[320],[1734],{"id":1735,"sortIndex":19,"affiliation":1736,"properties":18},"425959f4-2e67-40fc-a58c-0cb0a9e6598e",{"id":1735,"createTime":18,"updateTime":18,"relativeEntities":1737,"slug":18,"properties":1738,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":1741,"statistic":18},[],{"title":1739},{"EN":1740},"Department of Biology, McGill University, Montreal, Canada",[],{"title":1743},{"VI":1744},"Y. 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