Literature DB >> 10860668

Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32.

S Hayashida1, K Yamasaki, Y Asada, E Soeda, N Niikawa, T Kishino.   

Abstract

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 approximately 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. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10860668     DOI: 10.1006/geno.2000.6206

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  9 in total

Review 1.  Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.

Authors:  M P Hitchins; P Stanier; M A Preece; G E Moore
Journal:  J Med Genet       Date:  2001-12       Impact factor: 6.318

Review 2.  The genetics of the Silver-Russell syndrome.

Authors:  Michael A Preece
Journal:  Rev Endocr Metab Disord       Date:  2002-12       Impact factor: 6.514

3.  The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome.

Authors:  L Bentley; K Nakabayashi; D Monk; C Beechey; J Peters; Z Birjandi; F E Khayat; M Patel; M A Preece; P Stanier; S W Scherer; G E Moore
Journal:  J Med Genet       Date:  2003-04       Impact factor: 6.318

4.  A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

Authors: 
Journal:  Am J Hum Genet       Date:  2001-07-30       Impact factor: 11.025

5.  A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region.

Authors:  K Hannula; M Lipsanen-Nyman; T Kontiokari; J Kere
Journal:  Am J Hum Genet       Date:  2000-12-08       Impact factor: 11.025

Review 6.  Autism: in search of susceptibility genes.

Authors:  Janine A Lamb; Jeremy R Parr; Anthony J Bailey; Anthony P Monaco
Journal:  Neuromolecular Med       Date:  2002       Impact factor: 3.843

7.  The novel imprinted carboxypeptidase A4 gene ( CPA4) in the 7q32 imprinting domain.

Authors:  Tomohiko Kayashima; Kentaro Yamasaki; Takahiro Yamada; Hideki Sakai; Nobutomo Miwa; Tohru Ohta; Koh-ichiro Yoshiura; Naomichi Matsumoto; Yoshibumi Nakane; Hiroshi Kanetake; Fumitoshi Ishino; Norio Niikawa; Tatsuya Kishino
Journal:  Hum Genet       Date:  2003-01-28       Impact factor: 4.132

8.  Prostate cancer aggressiveness locus on chromosome 7q32-q33 identified by linkage and allelic imbalance studies.

Authors:  Phillippa J Neville; David V Conti; Pamela L Paris; Howard Levin; William J Catalona; Brian K Suarez; John S Witte; Graham Casey
Journal:  Neoplasia       Date:  2002 Sep-Oct       Impact factor: 5.715

Review 9.  BACs as tools for the study of genomic imprinting.

Authors:  S J Tunster; M Van De Pette; R M John
Journal:  J Biomed Biotechnol       Date:  2010-12-13
  9 in total

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