Roessler E, Ward D E, Gaudenz K, Belloni E, Scherer S W, Donnai D, Siegel-Bartelt J, Tsui L C, Muenke M
Children's Hospital of Philadelphia, Department of Pediatrics and Genetics, University of Pennsylvania School of Medicine, Philadelphia 19104-4399, USA.
Hum Genet. 1997 Aug;100(2):172-81. doi: 10.1007/s004390050486.
Holoprosencephaly (HPE) is a genetically heterogeneous disorder that affects the midline development of the forebrain and midface in humans. As a step toward identifying one of the HPE genes, we have set out to refine the HPE3 critical region on human chromosome 7q36 by analyzing 34 cell lines from families with cytogenetic abnormalities involving 7q, 24 of which are associated with HPE. Genomic clones surrounding the DNA marker D7S104, which has previously been shown to be in the HPE3 critical region, have been examined by fluorescent in situ hybridization and microsatellite analysis of our panel of patient cell lines. We report the analysis of a cluster of four translocation breakpoints within a 300-kb region of 7q36 that serves to define the minimal critical region for HPE3 and that has directed the search for candidate genes. The human Sonic Hedgehog (hSHH) gene maps to this region and has been shown to be HPE3 on the basis of mutations within the coding region of the gene. We present evidence that cytogenetic deletions and/or rearrangements of this region of chromosome 7q containing Sonic Hedgehog, and translocations that may suppress Sonic Hedgehog gene expression through a position effect are common mechanisms leading to HPE.
前脑无裂畸形(HPE)是一种基因异质性疾病,会影响人类前脑和中面部的中线发育。作为鉴定HPE相关基因之一的一个步骤,我们已着手通过分析来自涉及7q染色体细胞遗传学异常家庭的34个细胞系来细化人类7q36染色体上的HPE3关键区域,其中24个与HPE相关。围绕DNA标记D7S104(先前已证明其位于HPE3关键区域)的基因组克隆,已通过荧光原位杂交以及我们的患者细胞系面板的微卫星分析进行了检测。我们报告了对7q36染色体上一个300 kb区域内四个易位断点簇的分析,该区域用于定义HPE3的最小关键区域,并指导了对候选基因的搜索。人类音猬因子(hSHH)基因定位于该区域,并且基于该基因编码区域内的突变已证明其为HPE3。我们提供的证据表明,包含音猬因子的7q染色体该区域的细胞遗传学缺失和/或重排,以及可能通过位置效应抑制音猬因子基因表达的易位,是导致HPE的常见机制。