Literature DB >> 7533524

Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B.

F L Boldog1, B Waggoner, T W Glover, I Chumakov, D Le Paslier, D Cohen, R M Gemmill, H A Drabkin.   

Abstract

An extended YAC contig has been developed for the 3p14 region containing the hereditary renal carcinoma 3;8 translocation breakpoint and the 3p14.2 fragile site FRA3B. This region of chromosome 3 has been implicated by chromosomal translocation, deletion, and loss of heterozygosity in the pathogenesis of several malignant diseases. The contig allows accurate positioning of candidate genes, polymorphic markers, and other 3p rearrangements within this region. The contig, spanning approximately 6 Mb of DNA, contains 51 YACs identified by 27 markers, including a subset of CA repeats located in the 3p14.1-14.2 interval. The order of CA microsatellites, derived from marker content of the YACs, is in agreement with the order previously determined by genetic linkage studies. We find that the protein-tyrosine phosphatase gamma gene, PTPRG, is located minimally 1 Mb proximal to the t(3;8) breakpoint. The more proximal 3p homozygous deletion in the small-cell lung cancer cell line, U2020, is more than 5 Mb from the site of the 3;8 translocation. This integrated physical and genetic map provides a framework for further investigations of malignant diseases associated with proximal 3p loss. In addition, the positioning of separate 3p14.2 aphidicolin-induced breakpoints suggests that FRA3B may represent a region rather than a single site.

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Year:  1994        PMID: 7533524     DOI: 10.1002/gcc.2870110403

Source DB:  PubMed          Journal:  Genes Chromosomes Cancer        ISSN: 1045-2257            Impact factor:   5.006


  5 in total

Review 1.  Molecular characterization of common fragile sites as a strategy to discover cancer susceptibility genes.

Authors:  Larissa Savelyeva; Lena M Brueckner
Journal:  Cell Mol Life Sci       Date:  2014-09-18       Impact factor: 9.261

2.  The neurobeachin gene spans the common fragile site FRA13A.

Authors:  Larissa Savelyeva; Evgeny Sagulenko; Jens Guido Schmitt; Manfred Schwab
Journal:  Hum Genet       Date:  2005-10-22       Impact factor: 4.132

3.  Replication stress induces tumor-like microdeletions in FHIT/FRA3B.

Authors:  Sandra G Durkin; Ryan L Ragland; Martin F Arlt; Jennifer G Mulle; Stephen T Warren; Thomas W Glover
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-27       Impact factor: 11.205

4.  The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8.

Authors:  R M Gemmill; J D West; F Boldog; N Tanaka; L J Robinson; D I Smith; F Li; H A Drabkin
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-04       Impact factor: 11.205

5.  45S rDNA regions are chromosome fragile sites expressed as gaps in vitro on metaphase chromosomes of root-tip meristematic cells in Lolium spp.

Authors:  Jing Huang; Lu Ma; Fei Yang; Shui-zhang Fei; Lijia Li
Journal:  PLoS One       Date:  2008-05-14       Impact factor: 3.240

  5 in total

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