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Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32
被引:27
|作者:
Hayashida, S
Yamasaki, K
Asada, Y
Soeda, E
Niikawa, N
Kishino, T
机构:
[1] Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
[2] Nagasaki Univ, Sch Med, Dept Obstet & Gynecol, Nagasaki 8528523, Japan
[3] Inst Phys & Chem Res, RIKEN Gene Bank, Tsukuba, Ibaraki 305, Japan
来源:
关键词:
D O I:
10.1006/geno.2000.6206
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
MEST/PEG1, a gene expressed paternally in mesodermal derivatives in early embryonic stages, is the first imprinted gene mapped to chromosome 7q32. Since imprinted genes are clustered in general at a chromosomal region, we speculated that a similar imprinted-gene cluster may exist at chromosome region 7q32 and that the functions of some such genes may contribute to the phenotype of Silver-Russell syndrome including maternal uniparental disomy for chromosome 7 (maternal UPD7). As an initial step toward the isolation of imprinted genes at 7q32, we adopted an integrated approach involving the construction of a PAC contig and ESTs mapping in the vicinity of MEST. Here, we have constructed a complete contig of PAC and BAC clones and a transcript map spanning the entire similar to 1-Mb region between D7S530 and D7S649. We developed 60 novel STSs and precisely mapped 47 genes/ESTs. This map contains a putative autistic disorder locus that has been suggested to be localized near markers D7S530 and D7S684. This integrated physical and transcript map provides a valuable resource for identification of an imprinted gene(s) in this region as well as a candidate gene(s) for autistic disorder. (C) 2000 Academic Press.
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页码:221 / 225
页数:5
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