Literature DB >> 2268580

Irradiation microcell-mediated chromosome transfer (XMMCT): the generation of specific chromosomal arm deletions.

S F Dowdy1, D J Scanlon, C L Fasching, G Casey, E J Stanbridge.   

Abstract

The microcell-mediated chromosome transfer technique has been used to introduce whole chromosomes into malignant cells and revert the tumorigenic phenotype. However, in most instances the limited availability of selectable chromosomes has hindered the ability to reduce the region containing the tumor suppressive information. The work presented here describes a new method to enrich for specific chromosomal arm deletions of selectable chromosomes and thereby more finely focus upon the genetic region of interest. The irradiation-microcell mediated chromosome transfer (XMMCT) technique involves the irradiation of microcells containing single human chromosomes followed by fusion to a nonirradiated host and cytogenetic characterization. The XMMCT procedure was performed on a microcell hybrid containing a der(11) as the only human chromosome. The resultant irradiated microcell hybrids were found to have deletions that ranged from simple interstitial deletions to complex deletions/rearrangements involving only the human der(11) chromosome. The XMMCT procedure has broad applications in generating chromosomal reagents for mapping genetic loci and for use in functional analyses such as tumor suppression studies.

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Year:  1990        PMID: 2268580     DOI: 10.1002/gcc.2870020410

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


  7 in total

Review 1.  Microcell-mediated chromosome transfer (MMCT): small cells with huge potential.

Authors:  Aideen M O Doherty; Elizabeth M C Fisher
Journal:  Mamm Genome       Date:  2003-09       Impact factor: 2.957

2.  Chromosome specific c-DNA libraries: reduction of unspecific priming events by purification of heteronuclear RNA.

Authors:  P J Lagoda; J M Trent; E U Meese
Journal:  Mol Biol Rep       Date:  1994-03       Impact factor: 2.316

3.  Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24.

Authors:  S Matsuura; C Weemaes; D Smeets; H Takami; N Kondo; S Sakamoto; N Yano; A Nakamura; H Tauchi; S Endo; M Oshimura; K Komatsu
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

4.  Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene.

Authors:  J T Pang; S E Lloyd; C Wooding; B Farren; B Pottinger; B Harding; S E Leigh; M A Pook; F J Benham; G T Gillett; R T Taggart; R V Thakker
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

5.  Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering.

Authors:  Satoshi Abe; Hiromi Tanaka; Tomomi Notsu; Shin-Ichi Horike; Chikako Fujisaki; Dong-Lai Qi; Takahito Ohhira; David Gilley; Mitsuo Oshimura; Hiroyuki Kugoh
Journal:  Genome Integr       Date:  2010-05-26

6.  EagI and NotI linking clones from human chromosomes 11 and Xp.

Authors:  M A Pook; R Thakrar; B Pottinger; B Harding; D Porteous; V van Heyningen; J Cowell; C Jones; S Povey; K E Davies; R V Thakker
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

7.  Subchromosomal mapping of a putative transformation suppressor gene on human chromosome 1.

Authors:  I Horikawa; H Yamada; H Kugoh; Y Yuasa; M Suzuki; M Oshimura
Journal:  Jpn J Cancer Res       Date:  1995-05
  7 in total

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