Literature DB >> 8750194

An integrated map of human chromosome 6p23.

M G Olavesen1, A F Davies, S J Broxholme, J L Wixon, G Senger, D Nizetic, R D Campbell, J Ragoussis.   

Abstract

The human chromosomal band 6p23 is a Giemsa-negative (light) band that may be expected to be relatively gene rich. The genes for spinocerebellar ataxia type 1 (SCA1), guanosine monophosphate reductase (GMPR), DEK involved in a subtype of acute myeloid leukemia (AML), and the folate-sensitive fragile site FRA6A, have already been mapped to 6p23. Recent linkage data have suggested evidence for a susceptibility locus for schizophrenia in the region. We have constructed a single YAC contig of approximately 100 clones spanning the entire 6p23 band from 6p22.3 to 6p24.1 and covering 7.5-8.5 Mb of DNA. The YAC contig contains 55 markers including genetically mapped STSs, physically mapped STSs, anonymous STSs, anonymous ESTs, and ESTs from the genes mapped to the region. The order of the genetically mapped STSs is consistent with their order in the contig and some of the markers not resolved on the genetic map have been resolved by the YACs. Four of the YACs from 6p23 and covering approximately 3 Mb of DNA have been used to isolate approximately 300 cosmids from a flow-sorted human chromosome 6 cosmid library, which have been organized into pockets. The proposed susceptibility locus for schizophrenia is most closely linked to D6S260, which is located within the YAC contig along with genetic markers < or = 5 cM on either side. Therefore, the presented materials are valuable reagents for characterization of the genomic region implicated in schizophrenia.

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Year:  1995        PMID: 8750194     DOI: 10.1101/gr.5.4.342

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


  4 in total

Review 1.  Fragility Extraordinaire: Unsolved Mysteries of Chromosome Fragile Sites.

Authors:  Wenyi Feng; Arijita Chakraborty
Journal:  Adv Exp Med Biol       Date:  2017       Impact factor: 2.622

2.  Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting.

Authors:  A F Davies; K Imaizumi; G Mirza; R S Stephens; Y Kuroki; M Matsuno; J Ragoussis
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

3.  Physical map of human 6p21.2-6p21.3: region flanking the centromeric end of the major histocompatibility complex.

Authors:  N Tripodis; R Mason; S J Humphray; A F Davies; J A Herberg; J Trowsdale; D Nizetic; G Senger; J Ragoussis
Journal:  Genome Res       Date:  1998-06       Impact factor: 9.043

Review 4.  Are common fragile sites merely structural domains or highly organized "functional" units susceptible to oncogenic stress?

Authors:  Alexandros G Georgakilas; Petros Tsantoulis; Athanassios Kotsinas; Ioannis Michalopoulos; Paul Townsend; Vassilis G Gorgoulis
Journal:  Cell Mol Life Sci       Date:  2014-09-20       Impact factor: 9.261

  4 in total

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