Literature DB >> 9253597

A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb.

G G Bouffard1, J R Idol, V V Braden, L M Iyer, A F Cunningham, L A Weintraub, J W Touchman, R M Mohr-Tidwell, D C Peluso, R S Fulton, M S Ueltzen, J Weissenbach, C L Magness, E D Green.   

Abstract

The construction of highly integrated and annotated physical maps of human chromosomes represents a critical goal of the ongoing Human Genome Project. Our laboratory has focused on developing a physical map of human chromosome 7, a approximately 170-Mb segment of DNA that corresponds to an estimated 5% of the human genome. Using a yeast artificial chromosome (YAC)-based sequence-tagged site (STS)-content mapping strategy, 2150 chromosome 7-specific STSs have been established and mapped to a collection of YACs highly enriched for chromosome 7 DNA. The STSs correspond to sequences generated from a variety of DNA sources, with particular emphasis placed on YAC insert ends, genetic markers, and genes. The YACs include a set of relatively nonchimeric clones from a human-hamster hybrid cell line as well as clones isolated from total genomic libraries. For map integration, we have localized 260 STSs corresponding to Genethon genetic markers and 259 STSs corresponding to markers orders by radiation hybrid (RH) mapping on our YAC contigs. Analysis of the data with the program SEGMAP results in the assembly of 22 contigs that are "anchored" on the Genethon genetic map, the RH map, and/or the cytogenetic map. These 22 contigs are ordered relative to one another, are (in all but 3 cases) oriented relative to the centromere and telomeres, and contain > 98% of the mapped STSs. The largest anchored YAC contig, accounting for most of 7p, contains 634 STSs and 1260 YACs. An additional 14 contigs, accounting for approximately 1.5% of the mapped STSs, are assembled but remain unanchored on either the genetic or RH map. Therefore, these 14 "orphan" contigs are not ordered relative to other contigs. In our contig maps, adjacent STSs are connected by two or more YACs in > 95% of cases. With 2150 mapped STSs, our map provides an average STS spacing of approximately 79 kb. The physical map we report here exceeds the goal of 100-kb average STS spacing and should provide an excellent framework for systematic sequencing of the chromosome.

Entities:  

Mesh:

Year:  1997        PMID: 9253597     DOI: 10.1101/gr.7.7.673

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  24 in total

1.  An integrated physical map for the short arm of human chromosome 5.

Authors:  E T Peterson; R Sutherland; D L Robinson; L Chasteen; M Gersh; J Overhauser; L L Deaven; R K Moyzis; D L Grady
Journal:  Genome Res       Date:  1999-12       Impact factor: 9.043

2.  Leishmania major Friedlin chromosome 1 has an unusual distribution of protein-coding genes.

Authors:  P J Myler; L Audleman; T deVos; G Hixson; P Kiser; C Lemley; C Magness; E Rickel; E Sisk; S Sunkin; S Swartzell; T Westlake; P Bastien; G Fu; A Ivens; K Stuart
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-16       Impact factor: 11.205

3.  Construction of a high-resolution physical map of the approximate 1-Mb region of human chromosome 7q31.1-q31.2 harboring a putative tumor suppressor gene.

Authors:  J C Zenklusen; L A Weintraub; E D Green
Journal:  Neoplasia       Date:  1999-04       Impact factor: 5.715

4.  A major locus for myoclonus-dystonia maps to chromosome 7q in eight families.

Authors:  C Klein; K Schilling; R J Saunders-Pullman; J Garrels; X O Breakefield; M F Brin; D deLeon; D Doheny; S Fahn; J S Fink; L Forsgren; J Friedman; S Frucht; J Harris; G Holmgren; B Kis; R Kurlan; M Kyllerman; A E Lang; J Leung; D Raymond; J D Robishaw; G Sanner; E Schwinger; R E Tabamo; M Tagliati
Journal:  Am J Hum Genet       Date:  2000-10-05       Impact factor: 11.025

5.  Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes.

Authors:  R E Ellsworth; D C Jamison; J W Touchman; S L Chissoe; V V Braden Maduro; G G Bouffard; N L Dietrich; S M Beckstrom-Sternberg; L M Iyer; L A Weintraub; M Cotton; L Courtney; J Edwards; R Maupin; P Ozersky; T Rohlfing; P Wohldmann; T Miner; K Kemp; J Kramer; I Korf; K Pepin; L Antonacci-Fulton; R S Fulton; P Minx; L W Hillier; R K Wilson; R H Waterston; W Miller; E D Green
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-01       Impact factor: 11.205

6.  A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23.

Authors:  R Peoples; Y Franke; Y K Wang; L Pérez-Jurado; T Paperna; M Cisco; U Francke
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

7.  A composite-likelihood approach for detecting directional selection from DNA sequence data.

Authors:  Lan Zhu; Carlos D Bustamante
Journal:  Genetics       Date:  2005-05-06       Impact factor: 4.562

8.  Estimation of DNA sequence context-dependent mutation rates using primate genomic sequences.

Authors:  Wei Zhang; Gerard G Bouffard; Susan S Wallace; Jeffrey P Bond
Journal:  J Mol Evol       Date:  2007-08-04       Impact factor: 2.395

9.  Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder.

Authors:  Jacquelyn R Idol; Anjene M Addington; Robert T Long; Judith L Rapoport; Eric D Green
Journal:  J Autism Dev Disord       Date:  2007-09-19

10.  A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.

Authors:  D Johnson; S W Horsley; D M Moloney; M Oldridge; S R Twigg; S Walsh; M Barrow; P R Njølstad; J Kunz; G J Ashworth; S A Wall; L Kearney; A O Wilkie
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.