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与人类BRCA1基因呈头对头排列的NBR2基因的分离与鉴定。

Isolation and characterisation of the NBR2 gene which lies head to head with the human BRCA1 gene.

作者信息

Xu C F, Brown M A, Nicolai H, Chambers J A, Griffiths B L, Solomon E

机构信息

Somatic Cell Genetics Laboratory, Imperial Cancer Research Fund, London, UK.

出版信息

Hum Mol Genet. 1997 Jul;6(7):1057-62. doi: 10.1093/hmg/6.7.1057.

Abstract

To study the regulation of BRCA1 gene expression and the potential importance of dysregulation of this gene in breast and ovarian cancer, we have examined the 5' region of the human BRCA1 gene in detail. We have identified a new gene, NBR2, which is partially related to the NBR1 gene (formerly known as 1A1-3B and mapping directly adjacent to the pseudo-BRCA1 gene) and which lies head to head with the BRCA1 gene. The physical distance between the transcription start sites of the NBR2 and BRCA1 genes is 218 bp, suggesting that regulation of the expression of both genes may be co-ordinated through a bi-directional promoter. The NBR2 gene contains five exons spanning a genomic region of approximately 30 kb between the BRCA1 and pseudo-BRCA1 genes. Northern analysis showed that the NBR2 gene is expressed in all the tissues examined. The NBR2 cDNA contains an open reading frame of 112 amino acids and is predicted to encode a protein of approximately 12 kDa. Single-strand conformation polymorphism (SSCP) analysis of the NBR2 gene failed to identify any mutations in either breast or ovarian cancer, suggesting that if the NBR2 gene is involved in the development of these cancers, other mechanisms for tumorigenesis may exist. Hybridisation of NBR2 probes to zoo blots showed that the NBR2 gene is present in human and other primates. No hybridisation to DNA from other species was observed, suggesting that genomic elements controlling BRCA1 expression may differ between species.

摘要

为了研究BRCA1基因表达的调控以及该基因失调在乳腺癌和卵巢癌中的潜在重要性,我们详细检测了人类BRCA1基因的5'区域。我们鉴定出一个新基因NBR2,它与NBR1基因(以前称为1A1 - 3B,直接定位于假BRCA1基因相邻位置)部分相关,并且与BRCA1基因头对头排列。NBR2基因和BRCA1基因转录起始位点之间的物理距离为218 bp,这表明两个基因的表达调控可能通过双向启动子进行协调。NBR2基因包含五个外显子,跨越BRCA1基因和假BRCA1基因之间约30 kb的基因组区域。Northern分析表明,NBR2基因在所检测的所有组织中均有表达。NBR2 cDNA包含一个112个氨基酸的开放阅读框,预计编码一种约12 kDa的蛋白质。对NBR2基因进行单链构象多态性(SSCP)分析,未在乳腺癌或卵巢癌中发现任何突变,这表明如果NBR2基因参与这些癌症的发生发展,可能存在其他肿瘤发生机制。用NBR2探针与动物印迹杂交表明,NBR2基因存在于人类和其他灵长类动物中。未观察到与其他物种DNA的杂交信号,这表明控制BRCA1表达的基因组元件在不同物种之间可能存在差异。

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