Sequence analysis of translationally controlled maternal mRNAs from Urechis caupo

Wiley - Tập 14 Số 6 - Trang 485-491 - 1993
Eric T. Rosenthal1
1Pacific Bioomedical Research Center, Kewalo Marine Laboratory, University of Hawaii, Honolulu

Tóm tắt

AbstractFertilization of Urechis coupo oocytes stimulates dramatic changes in the pattern of protein synthesis. This shift is brought about entirely through selective translation of the large pool of maternal mRNAs synthesized and stored during oogenesis. My laboratory has identified cDNA clones to more than 20 different Urechis maternal mRNAs. These have been used to determine whether the complementary mRNAs are translated in oocytes or embryos, and to analyze the polyad‐enylation status of the mRNAs at different stages. For 14 of the mRNAs, multiple, overlapping cDNA clones were isolated, and the complete sequence of the mRNA molecule was determined. Of these 14 mRNAs, half are from the subset that is translated in growing and full‐grown oocytes, but not in embryos. These 7 mRNAs have poly(A) tails before fertilization. The other 7 are from the subset that is not translated at any time before fertilization, and has very short poly(A) tails in oocytes. After fertilization these mRNAs are recruited onto polysomes and extensively polyadenylated. The sequence data from the two classes of maternal mRNAs was compared in an attempt to identify consensus sequences that could regulate translation directly, or indirectly, by controlling polyadenylation or secondary structure formation. Two features of the sequences correlate very well with the translation and polyadenylation of the different mRNAs‐the identity of the base immediately preceding the AUG start codon, and the presence of the sequences UUUUA and UUUUUA in the 3′ untranslated region. © 1993 Wiley‐Liss, Inc.

Từ khóa


Tài liệu tham khảo

10.1016/S0022-2836(05)80360-2

10.1128/MCB.8.4.1591

10.1093/nar/19.12.3185

10.1016/0003-2697(83)90418-9

10.1128/MCB.11.4.2149

10.1101/gad.3.12b.2151

10.1101/gad.4.12b.2287

10.1101/gad.2.5.598

10.1016/0092-8674(90)90235-7

10.1016/0092-8674(93)90290-7

10.1083/jcb.88.3.604

Kozak M, 1986, Point mutations define a sequence flanking the AUG initiator codon that modulates translation by cukaryolic ribosomes, Cell, 44, 283, 10.1016/0092-8674(86)90762-2

10.1016/0022-2836(87)90418-9

10.1128/MCB.8.7.2737

10.1083/jcb.108.2.229

10.1128/MCB.9.11.5073

10.1083/jcb.115.4.887

10.1146/annurev.cb.08.110192.001213

LazT ClementsJ Sherman F(1987):The role of messenger RNA sequences and structures in eukaryotic translation. In Ilan J (ed): “Translational Regulation of Gene Expression.”

10.1002/j.1460-2075.1987.tb04716.x

10.1101/gad.3.6.803

McGrew LL, 1990, Translational control by cytoplasmic polyadenylation during Xenopus oocyte maturation: Characterization of cis and trans elements and regulation by cyclin/MPF, EMBO J, 9, 3643, 10.1002/j.1460-2075.1990.tb07587.x

McSwiggin JA, 1990, RNA sequencing, Comments (USB, 17, 1

10.1016/0378-1119(90)90056-W

10.1128/MCB.10.11.5634

10.1073/pnas.85.8.2444

10.1002/bies.950130406

10.1016/0012-1606(86)90347-7

RosenthalET WiltFH(1987):Selective mRNA translation in marine invertebrate oocytes eggs and embryos. In Ilan J (ed): “Translational Regulation of Gene Expression.”

Rosenthal ET, 1991, Distribution of the 34 kD laminin binding protein during Urechis development, J Cell Biol, 111, 23a

Rosenthal ET, 1993, Identification of homologues to β‐catenin/pla‐koglobin/armadillo in two invertebrates, Urechis caupo and Trip‐neustes gratilla, Biochirn Biophys Acta, 1173, 333

10.1006/dbio.1993.1029

10.1073/pnas.74.12.5463

Slatko B, 1992, Constructing nested deletions for use in DNA sequencing, Curr Protocols Mol Biol, 16, 7.2.1

Slatko B, 1992, DNA sequencing by the dideoxy method, Curr Protocols Mol Biol, 21, 7.4.1

10.1101/gad.4.12a.2157

United States Biochemicals, 1990, DNA Sequencing Guide

10.1101/gad.4.12b.2278

10.1101/gad.3.12b.2163