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膀胱外翻-尿道上裂复合畸形:在一大群患者中对异染色质抑制因子、zeste增强子和三胸节蛋白(SET)作为候选基因的研究。

Bladder exstrophy-epispadias complex: Investigation of suppressor of variegation, enhancer of zeste and Trithorax (SET) as a candidate gene in a large cohort of patients.

作者信息

Reutter Heiko, Thauvin-Robinet Christel, Boemers Thomas M, Rösch Wolfgang H, Ludwig Michael

机构信息

Department of Human Genetics, University of Bonn, Bonn, Germany.

出版信息

Scand J Urol Nephrol. 2006;40(3):221-4. doi: 10.1080/00365590600621204.

Abstract

OBJECTIVE

The bladder exstrophy-epispadias complex (BEEC) describes a rare anterior midline defect with variable expression involving the infra-umbilical abdominal wall, including the pelvis, urinary tract and external genitalia. It is assumed that the underlying cause of BEEC is a multifactorial mode of inheritance; however, its aetiology remains unknown. Only a few BEEC patients with distinctive cytogenetic features such as numeric or structural chromosomal abnormalities have been reported. The observation of translocations concerning the region of chromosome 9q32-q34.1 in two patients implies that this region bears a candidate gene which, during early blastogenesis, governs the development of this primary field. In this context, we considered the suppressor of variegation, enhancer of zeste and Trithorax (SET) gene, located at chromosome 9q34, to be a good candidate, as the protein encoded is involved in the regulation of cell proliferation and differentiation. Moreover, SET expression was detected in embryonic kidney.

MATERIAL AND METHODS

A total of 33 patients affected with BEEC were analysed for mutations in the SET gene.

RESULTS

SET analysis did not reveal either a mutation or the presence of four single-nucleotide polymorphisms (dbSNP124) already described in the database.

CONCLUSIONS

The data obtained in this study most likely exclude the SET gene as a possible genetic cause of BEEC. Hence, other genes in this region may contribute to the development of this midline defect.

摘要

目的

膀胱外翻-尿道上裂复合畸形(BEEC)是一种罕见的前正中线缺损,表现多样,累及脐下腹壁,包括骨盆、泌尿道和外生殖器。一般认为BEEC的潜在病因是多因素遗传模式;然而,其病因仍不明。仅有少数具有独特细胞遗传学特征(如染色体数目或结构异常)的BEEC患者被报道。两名患者中观察到涉及9号染色体q32-q34.1区域的易位,这意味着该区域存在一个候选基因,在早期胚泡形成过程中,该基因控制这一原基的发育。在此背景下,我们认为位于9号染色体q34的异染色质抑制因子、zeste增强子和三胸节蛋白(SET)基因是一个很好的候选基因,因为其编码的蛋白质参与细胞增殖和分化的调控。此外,在胚胎肾中检测到SET表达。

材料与方法

对33例BEEC患者进行SET基因突变分析。

结果

SET分析未发现数据库中已描述的突变或4个单核苷酸多态性(dbSNP124)。

结论

本研究获得的数据很可能排除SET基因是BEEC可能的遗传病因。因此,该区域的其他基因可能与这种中线缺损的发生有关。

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