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

被引:5
作者
Drouin, R
Boutouil, M
Fetni, R
Holmquist, GP
Scott, P
Richer, CL
Lemieux, N
机构
[1] UNIV LAVAL,DEPT PATHOL,QUEBEC CITY,PQ G1L 3L5,CANADA
[2] UNIV MONTREAL,FAC MED,DEPT PATHOL,MONTREAL,PQ H3C 3J7,CANADA
[3] CITY HOPE NATL MED CTR,BECKMAN RES INST,DEPT BIOL,DUARTE,CA 91010
[4] HOP ST JUSTINE,DEPT PATHOL,MONTREAL,PQ H3T 1C5,CANADA
[5] HOP ST JUSTINE,CTR RECH PEDIAT,MONTREAL,PQ H3T 1C5,CANADA
基金
英国医学研究理事会;
关键词
D O I
10.1007/s004120050262
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:405 / 411
页数:7
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