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小鼠16号染色体的一个区域与迪格奥尔格综合征、腭心面综合征的最小关键区域同线。

A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region.

作者信息

Galili N, Baldwin H S, Lund J, Reeves R, Gong W, Wang Z, Roe B A, Emanuel B S, Nayak S, Mickanin C, Budarf M L, Buck C A

机构信息

Wistar Institute, Philadelphia, Pennsylvania, USA.

出版信息

Genome Res. 1997 Jan;7(1):17-26. doi: 10.1101/gr.7.1.17.

Abstract

DGS and VCFS, haploinsufficiencies characterized by multiple craniofacial and cardiac abnormalities, are associated with a microdeletion of chromosome 22q11.2. Here we document synteny between a 150-kb region on mouse chromosome 16 and the most commonly deleted portion of 22q11.2. Seven genes, all of which are transcribed in the early mouse embryo, have been identified. Of particular interest are two serine/threonine kinase genes and a novel goosecoid-like homeobox gene (Gscl). Comparative sequence analysis of a 38-kb segment reveals similarities in gene content, order, exon composition, and transcriptional direction. Therefore, if deletion of these genes results in DGS/VCFS in humans, then haploinsufficiencies involving this region of chromosome 16 should recapitulate the developmental field defects characteristic of this syndrome.

摘要

DiGeorge综合征(DGS)和腭心面综合征(VCFS)是以多种颅面和心脏异常为特征的单倍剂量不足,与22q11.2染色体微缺失相关。在此,我们记录了小鼠16号染色体上一个150 kb区域与22q11.2最常缺失部分之间的同线性。已鉴定出7个基因,所有这些基因均在小鼠早期胚胎中转录。特别令人感兴趣的是两个丝氨酸/苏氨酸激酶基因和一个新的类鹅膏蕈碱同源框基因(Gscl)。对一个38 kb片段的比较序列分析揭示了基因含量、顺序、外显子组成和转录方向上的相似性。因此,如果这些基因的缺失导致人类出现DGS/VCFS,那么涉及16号染色体该区域的单倍剂量不足应该会重现该综合征特有的发育场缺陷。

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