DNA replication asynchrony between the paternal and maternal alleles of imprinted genes does not straddle the R/G transition

Chromosoma - Tập 106 - Trang 405-411 - 1997
Régen Drouin1, Mohamed Boutouil2, Raouf Fetni2, Gerald P. Holmquist3, Patrick Scott2, Claude-Lise Richer2, Nicole Lemieux2
1Unité de Recherche en Génétique Humaine et Moléculaire, Centre de Recherche, Pavillon Saint-François d’Assise,   CHUQ, 10 rue de l’Espinay, and Department of Pathology, Université Laval, Québec, Canada G1L 3L5, , CA
2Département de Pathologie, Faculté de Médecine, Université de Montréal, C.P. 6128, Succ. A, Montréal, Canada H3C 3J7, , CA
3Department of Biology, Beckman Research Institute of the City of Hope, Duarte, CA 91010-3000, USA, , US

Tóm tắt

Imprinted autosomal loci apparently reside in very large chromosomal domains that exhibit asynchrony in replication of homologous alleles during the DNA synthesis phase. Replication asynchrony can be cytogenetically visualized by a replication-banding discordance between homologous bands of a given pair of chromosomal homologs. The replication time of a chromosomal band at high resolution can be determined by blocking DNA synthesis at the R/G-band transition and using replication banding. The R/G transition reflects the transition from early (R-) to late (G- and C-) band DNA replication. We studied discordance between two groups of homologous chromosomal bands: (a) four bands, 6q26–27, 11p13, 11p15.5 and 15q11.2–12, each containing at least one imprinted gene; and (b) nine bands containing no known imprinted genes. Fifty pairs of chromosomes were analyzed at high resolution after R/G transition blocking and late 5-bromo-2′-deoxyuridine incorporation. The rate of discordance was the same for bands containing imprinted genes and for control bands. Both homologous bands of a pair replicate either before or after the R/G transition and do not straddle the R/G transition. Repression associated with imprinting does not appear to involve late replication at the band level of resolution. Tissue-specific inactivation is associated with DNA methylation and late replication, whereas allele-specific inactivation is associated with DNA methylation but not with delayed or late replication.