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MAD2B及其他有丝分裂纺锤体检查点基因的特性分析

Characterization of MAD2B and other mitotic spindle checkpoint genes.

作者信息

Cahill D P, da Costa L T, Carson-Walter E B, Kinzler K W, Vogelstein B, Lengauer C

机构信息

Program in Human Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21231, USA.

出版信息

Genomics. 1999 Jun 1;58(2):181-7. doi: 10.1006/geno.1999.5831.

Abstract

Aneuploidy is a characteristic of the majority of human cancers, and recent work has suggested that mitotic checkpoint defects play a role in its development. To further explore this issue, we isolated a novel human gene, MAD2B (MAD2L2), which is homologous to the spindle checkpoint gene MAD2 (MAD2L1). We determined the chromosomal localization of it and other spindle checkpoint genes, including MAD1L1, MAD2, BUB3, TTK (MPS1L1), and CDC20. In addition, we resolved the genomic intron-exon structure of the human BUB1 gene. We then searched for mutations in these genes in a panel of 19 aneuploid colorectal tumors. No new mutations were identified, suggesting that genes yet to be discovered are responsible for most of the checkpoint defects observed in aneuploid cancers.

摘要

非整倍体是大多数人类癌症的一个特征,最近的研究表明有丝分裂检查点缺陷在其发展过程中起作用。为了进一步探讨这个问题,我们分离出了一个新的人类基因MAD2B(MAD2L2),它与纺锤体检查点基因MAD2(MAD2L1)同源。我们确定了它以及其他纺锤体检查点基因的染色体定位,包括MAD1L1、MAD2、BUB3、TTK(MPS1L1)和CDC20。此外,我们解析了人类BUB1基因的基因组内含子-外显子结构。然后我们在一组19个非整倍体结直肠癌肿瘤中搜索这些基因的突变。未发现新的突变,这表明尚未发现的基因是导致在非整倍体癌症中观察到的大多数检查点缺陷的原因。

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