Literature DB >> 1427886

A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus.

K A Frazer1, M Boehnke, M L Budarf, R K Wolff, B S Emanuel, R M Myers, D R Cox.   

Abstract

We describe a high-resolution radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 (NF2) gene. Eighty-five hamster-human somatic cell hybrids generated by X-irradiation and cell fusion were used to generate the radiation hybrid map. The presence or absence of 18 human chromosome 22-specific markers was determined in each hybrid by using Southern blot hybridization. Sixteen of the 18 markers were distinguishable by X-ray breakage in the radiation hybrids. Analysis of these data using two different mathematical models and two different statistical methods resulted in a single framework map consisting of 8 markers ordered with odds greater than 1000:1. The remaining nonframework markers were all localized to regions consisting of two adjoining intervals on the framework map with odds greater than 1000:1. Based on the RH map, the NF2 region of chromosome 22, defined by the flanking markers D22S1 and D22S28, is estimated to span a physical distance of approximately 6 Mb and is the most likely location for 9 of the 18 markers studied: D22S33, D22S41, D22S42, D22S46, D22S56, LIF, D22S37, D22S44, and D22S15.

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Year:  1992        PMID: 1427886     DOI: 10.1016/s0888-7543(05)80154-5

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


  5 in total

1.  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

Review 2.  Irradiation and fusion gene transfer.

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

3.  Construction of radiation-reduced hybrids and their use in mapping of microclones from chromosome 10p11.2-q11.2.

Authors:  S Fujita; E Shin; T Nakamura; H Kurahashi; Y Kaneda; K Tanaka; T Mori; S Takai; I Nishisho
Journal:  Jpn J Hum Genet       Date:  1993-12

4.  Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome.

Authors:  H Kurahashi; K Akagi; K Karakawa; T Nakamura; J P Dumanski; T Sano; S Okada; S Takai; I Nishisho
Journal:  Hum Genet       Date:  1994-03       Impact factor: 4.132

5.  Structure of the human TIMP-3 gene and its cell cycle-regulated promoter.

Authors:  M Wick; R Härönen; D Mumberg; C Bürger; B R Olsen; M L Budarf; S S Apte; R Müller
Journal:  Biochem J       Date:  1995-10-15       Impact factor: 3.857

  5 in total

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