Human chromosome 3: High-resolution fluorescence in situ hybridization mapping of 40 unique NotI linking clones homologous to genes and cDNAs

被引:28
作者
Protopopov, AI
Gizatullin, RZ
Vorobieva, NV
Protopopova, MV
Kiss, C
Kashuba, VI
Klein, G
Kisselev, LL
Graphodatsky, AS
Zabarovsky, ER
机构
[1] KAROLINSKA INST,DEPT TUMOR BIOL,S-17177 STOCKHOLM,SWEDEN
[2] RUSSIAN ACAD SCI,INST CYTOL & GENET,SIBERIAN BRANCH,NOVOSIBIRSK 630090,RUSSIA
[3] RUSSIAN ACAD SCI,ENGELHARDT INST MOL BIOL,MOSCOW,RUSSIA
[4] UKRAINIAN ACAD SCI,INST MOL BIOL & GENET,UA-252627 KIEV,UKRAINE
关键词
fluorescence in situ hybridization; human chromosome 3; localization of genes; Notl linking clones;
D O I
10.1007/BF02265051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Forty new Notl linking clones representing sequence tagged sites (STSs) were mapped by fluorescence in site hybridization (FISH) to different regions of human chromosome 3 (HSA3). Clone NL1-245, containing human aminoacylase 1, was localized to 3p21.2-p21.1. Our previous localization of the CLC-2 chloride channel protein gene was refined to 3q27. Clone NL2-316 most likely contains a translocon-associated protein gamma-subunit gene and was mapped to 3q23-q24. To our knowledge, this is the first time this gene has been mapped. One Notl linking clone (NL1-229) probably contains a new protein phosphatase gene. This clone was mapped to 3p25. Five Notl linking clones probably contain human expressed sequence tags (ESTs), as they possess sequences with a high level of identity (> 90%) to cDNA clones. Other clones show 56-85% homology to known mammalian and human genes with various functions, including oncogenes and tumour-suppressor genes. These clones might represent new genes.
引用
收藏
页码:443 / 447
页数:5
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