Alley T L, Gray B A, Lee S H, Scherer S W, Tsui L C, Tint G S, Williams C A, Zori R, Wallace M R
Department of Pediatrics, Division of Genetics, University of Florida College of Medicine, Gainesville, USA.
Am J Hum Genet. 1995 Jun;56(6):1411-6.
Smith-Lemli-Opitz syndrome (SLOS) is a mental retardation/multiple congenital anomaly syndrome. The gene(s) involved has not been mapped or cloned, but, recently, a biochemical abnormality in cholesterol biosynthesis has been shown to occur in most SLOS patients. The defect is suspected to occur in the penultimate step of the cholesterol pathway, involving the enzyme 7-dehydrocholesterol reductase, which has not been isolated. On the basis of the hypothesis that a de novo balanced translocation [t(7;20)(q32.1;q13.2)] in an SLOS patient directly interrupts the SLOS gene, positional cloning techniques are being employed to localize and identify the SLOS gene. We report the identification of a chromosome 7-specific YAC that spans the translocation breakpoint, as detected by FISH. This is the first study narrowing a candidate SLOS region and placing it on physical and genetic maps of the human genome.
史密斯-勒米-奥皮茨综合征(SLOS)是一种智力发育迟缓/多发先天性异常综合征。相关基因尚未定位或克隆,但最近研究表明,大多数SLOS患者存在胆固醇生物合成的生化异常。该缺陷疑似发生在胆固醇合成途径的倒数第二步,涉及尚未分离出来的7-脱氢胆固醇还原酶。基于一个SLOS患者的新生平衡易位[t(7;20)(q32.1;q13.2)]直接打断SLOS基因的假说,目前正在采用定位克隆技术来定位和鉴定SLOS基因。我们报告了通过荧光原位杂交(FISH)检测到的一个跨越易位断点的7号染色体特异性酵母人工染色体(YAC)的鉴定。这是首次将候选SLOS区域缩小并定位到人类基因组物理图谱和遗传图谱上的研究。