Literature DB >> 8244380

A radiation hybrid map of the BRCA1 region of chromosome 17q12-q21.

K J Abel1, M Boehnke, M Prahalad, P Ho, W L Flejter, M Watkins, J VanderStoep, S C Chandrasekharappa, F S Collins, T W Glover.   

Abstract

The chromosomal region 17q12-q21 contains a gene (BRCA1) conferring susceptibility to early-onset familial breast and ovarian cancer. An 8000-rad radiation-reduced hybrid (RH) panel was constructed to provide a resource for long-range mapping of this region. A large fraction of the hybrids (approximately 90%) retained detectable human chromosome 17 sequences. The complete panel of 76 hybrids was scored for the presence or absence of 22 markers from this chromosomal region, including 14 cloned genes, seven microsatellite repeats, and one anonymous DNA segment. Statistical analysis of the marker retention data employing multipoint methods provided both comprehensive and framework maps of this chromosomal region, including distance estimates between adjacent markers. The comprehensive RH map includes 17 loci and spans 179 cRays(8000). Likelihood ratios of at least 1000:1 support the 10-locus framework order: cen-D17S250-ERBB2-(THRA1, TOP2A)-D17S855-PPY-D17S190-MTBT1-GP3A++ +-BTR-D17S588-tel. The order obtained from RH mapping, when used in conjunction with other methods, will be useful in linkage analysis of breast cancer families and will facilitate the development of a physical map of this region.

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Year:  1993        PMID: 8244380     DOI: 10.1006/geno.1993.1383

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


  10 in total

1.  Low Frequency Loss of Heterozygosity in the BRCA1 Region in Japanese Sporadic Breast Cancer.

Authors: 
Journal:  Breast Cancer       Date:  1996-12-20       Impact factor: 4.239

2.  Biological indices in the assessment of breast cancer.

Authors:  A S Leong; A K Lee
Journal:  Clin Mol Pathol       Date:  1995-10

3.  A radiation hybrid map spanning the entire human X chromosome integrating YACs, genes, and STS markers.

Authors:  J Kumlien; A Grigoriev; H Roest Crollius; M Ross; P N Goodfellow; H Lehrach
Journal:  Mamm Genome       Date:  1996-10       Impact factor: 2.957

4.  Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.

Authors:  J R Murrell; D Koller; T Foroud; M Goedert; M G Spillantini; H J Edenberg; M R Farlow; B Ghetti
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

Review 5.  Irradiation and fusion gene transfer.

Authors:  M A Walter; P N Goodfellow
Journal:  Mol Biotechnol       Date:  1995-04       Impact factor: 2.695

6.  Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.

Authors:  K C Wilhelmsen; T Lynch; E Pavlou; M Higgins; T G Nygaard
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

7.  A radiation hybrid map of the BRCA1 region.

Authors:  P O'Connell; H Albertsen; N Matsunami; T Taylor; J E Hundley; T L Johnson-Pais; B Reus; E Lawrence; L Ballard; R White
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025

Review 8.  Transcript identification in the BRCA1 candidate region.

Authors:  B L Weber; K J Abel; F J Couch; S Merajver; L Castilla; L C Brody; F S Collins
Journal:  Breast Cancer Res Treat       Date:  1995       Impact factor: 4.872

Review 9.  Microdissection and microcloning of chromosomal alterations in human breast cancer.

Authors:  J M Trent; B Weber; X Y Guan; J Zhang; F Collins; K Abel; A Diamond; P Meltzer
Journal:  Breast Cancer Res Treat       Date:  1995       Impact factor: 4.872

10.  Direct visualization of the highly polymorphic RNU2 locus in proximity to the BRCA1 gene.

Authors:  Chloé Tessereau; Monique Buisson; Nastasia Monnet; Marine Imbert; Laure Barjhoux; Caroline Schluth-Bolard; Damien Sanlaville; Emmanuel Conseiller; Maurizio Ceppi; Olga M Sinilnikova; Sylvie Mazoyer
Journal:  PLoS One       Date:  2013-10-11       Impact factor: 3.240

  10 in total

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