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从人类染色体3p21.1区域分离出两个重叠黏粒的重叠群,并鉴定出5个新的3p21.1基因。

Isolation of two contigs of overlapping cosmids derived from human chromosomal band 3p21.1 and identification of 5 new 3p21.1 genes.

作者信息

Shridhar V, Golembieski W, Kamat A, Smith S E, Phillips N, Miller O J, Miller Y, Smith D I

机构信息

Wayne State University, School of Medicine, Detroit, Michigan 48201.

出版信息

Somat Cell Mol Genet. 1994 Jul;20(4):255-65. doi: 10.1007/BF02254716.

Abstract

Consistent loss of DNA sequences from several regions on the short arm of human chromosome 3 has suggested that multiple tumor suppressor genes reside on chromosome 3p in various types of cancer cells. We have focused our efforts on an analysis of chromosomal band 3p21.1 since aminoacylase-1 (ACY1), which is localized to this band, has been shown to have lower levels of expression in several small cell and non-small cell lung cancer cell lines. Starting with two cosmids within 3p21.1, D3S92 and D3S93, we have isolated two separate contigs of overlapping cosmids within 3p21.1, by screening a library of 5700 chromosome 3-specific cosmid clones. Detailed restriction maps for these two contigs show that they contain multiple clusters of rare cutting restriction endonuclease sites. One contig extends for 100 kb and encompassed both ACY1 and D3S92, and the other extends about 80 kb around the D3S93 locus. Many different restriction fragments derived from these two contigs were found to be evolutionarily conserved and hybridized to distinct message transcripts. These fragments were used to identify homologous cDNAs from an adenogastric cDNA library, and several of these cDNAs were partially sequenced. We have identified five new genes from these two contigs and there is evidence to suggest that several additional genes reside within these cosmid contigs. The genes identified from 3p21.1 were then hybridized to DNA, isolated from a series of lung cancer cell lines and matched normal and tumor DNA from lung cancer patients. No alterations were detected with any of these probes, both at the DNA or RNA levels. A similar analysis with DNA fragments derived from these two genomic regions also failed to detect any alterations.

摘要

人类3号染色体短臂上几个区域的DNA序列持续缺失,这表明多种肿瘤抑制基因存在于各类癌细胞的3号染色体短臂(3p)上。我们将研究重点放在了对染色体带3p21.1的分析上,因为定位于此带的氨酰基酶-1(ACY1)在几种小细胞和非小细胞肺癌细胞系中的表达水平较低。从3p21.1区域内的两个黏粒D3S92和D3S93入手,我们通过筛选一个包含5700个3号染色体特异性黏粒克隆的文库,分离出了3p21.1区域内两个独立的重叠黏粒重叠群。这两个重叠群的详细限制性图谱显示,它们包含多个稀有切割限制性内切酶位点簇。一个重叠群延伸100 kb,包含ACY1和D3S92,另一个围绕D3S93基因座延伸约80 kb。发现源自这两个重叠群的许多不同限制性片段在进化上是保守的,并与不同的信使转录本杂交。这些片段被用于从腺胃癌cDNA文库中鉴定同源cDNA,其中几个cDNA进行了部分测序。我们从这两个重叠群中鉴定出了五个新基因,并且有证据表明这些黏粒重叠群中还存在其他几个基因。然后将从3p21.1鉴定出的基因与从一系列肺癌细胞系中分离的DNA以及肺癌患者匹配的正常和肿瘤DNA进行杂交。在DNA或RNA水平上使用这些探针均未检测到任何改变。对源自这两个基因组区域的DNA片段进行的类似分析也未能检测到任何改变。

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