Jones Hazel C, Yehia Baligh, Chen Gin-Fu, Carter Barbara J
Department of Pharmacology and Therapeutics, University of Florida, Gainesville, FL 32610-0267, USA.
Exp Neurol. 2004 Nov;190(1):79-90. doi: 10.1016/j.expneurol.2004.06.019.
Congenital hydrocephalus is a serious neurological disorder with a diverse etiology. Although there is strong evidence for genetic causes, few genes have been identified in humans. The rodent model, the H-Tx rat, has hydrocephalus with an onset in late gestation and a complex mode of inheritance. Ventricular dilatation is associated with abnormalities in the cerebral aqueduct and subcommissural organ. Quantitative trait locus (QTL) mapping was performed on DNA from the progeny of a backcross with the non-hydrocephalic Fischer F344 strain, using DNA microsatellite markers. The hydrocephalus trait was quantified by measuring the severity of the ventricular dilatation. Four chromosomes, each with a locus for hydrocephalus (Chrs 9, 10, 11, and 17), were mapped using additional markers and DNA from four subsets of backcross progeny with allelic recombination at or near each locus. The genetic positions for the markers and the loci were located using the Ensemble Rat Genome Browser. For each chromosome studied, the interval containing the locus was examined for known rat genes and for human genes identified from human-rat homology. Genes expressed in brain and with a function associated with known causes of hydrocephalus were identified as possible candidate genes. Future studies to characterize the causative genes in this animal model will improve the understanding of genetic causes in humans.
先天性脑积水是一种病因多样的严重神经系统疾病。尽管有充分证据表明其由遗传因素导致,但在人类中仅鉴定出少数相关基因。啮齿动物模型H-Tx大鼠患有脑积水,发病于妊娠晚期,遗传模式复杂。脑室扩张与中脑导水管及连合下器官的异常有关。利用DNA微卫星标记,对与非脑积水的Fischer F344品系回交后代的DNA进行数量性状基因座(QTL)定位。通过测量脑室扩张的严重程度对脑积水性状进行量化。使用额外的标记以及来自回交后代四个子集的DNA(每个子集在每个基因座或其附近发生等位基因重组),对四条各带有一个脑积水基因座的染色体(第9、10、11和17号染色体)进行定位。利用Ensemble大鼠基因组浏览器确定标记和基因座的遗传位置。对于所研究的每条染色体,检查包含该基因座的区间,以查找已知的大鼠基因以及通过人鼠同源性鉴定出的人类基因。在脑中表达且功能与已知脑积水病因相关的基因被确定为可能的候选基因。未来对该动物模型中致病基因进行表征的研究将增进对人类遗传病因的理解。