Fournier B, Saudubray J M, Benichou B, Lyonnet S, Munnich A, Clevers H, Poll-The B T
University Children's Hospital Wilhelmina Kinderziekenhuis, University Hospital Utrecht, The Netherlands.
J Clin Invest. 1994 Aug;94(2):526-31. doi: 10.1172/JCI117365.
We have cloned the cDNA encoding human peroxisomal acyl-CoA oxidase, the first enzyme in the peroxisomal beta-oxidation of very long chain fatty acids. Its nucleotide sequence was found to be highly homologous (85%) to the rat cDNA counterpart. An 88% homology between rat and human was found in the COOH-terminal end of the cDNA which includes the Ser-Lys-Leu peroxisomal targeting signal common to many peroxisomal proteins. The gene spans approximately 30-40 kb and is poorly polymorphic. Southern blot analyses were performed in two previously reported siblings with an isolated peroxisomal acyl-CoA oxidase deficiency (pseudoneonatal adrenoleukodystrophy). A deletion of at least 17 kb, starting down-stream from exon 2 and extending beyond the 3' end of the gene, was observed in the two patients. These observations provide a molecular basis for the observed acyl-CoA oxidase deficiency in our family. In addition, our study will enable the characterization of the genetic defect in unrelated families with suspected acyl-CoA oxidase disorders.
我们已经克隆了编码人过氧化物酶体酰基辅酶A氧化酶的cDNA,该酶是极长链脂肪酸过氧化物酶体β氧化的首个酶。发现其核苷酸序列与大鼠cDNA对应序列高度同源(85%)。在cDNA的COOH末端发现大鼠和人之间有88%的同源性,该末端包含许多过氧化物酶体蛋白共有的丝氨酸-赖氨酸-亮氨酸过氧化物酶体靶向信号。该基因跨度约为30-40kb,多态性较低。对先前报道的两名患有孤立性过氧化物酶体酰基辅酶A氧化酶缺乏症(假性新生儿肾上腺脑白质营养不良)的同胞进行了Southern印迹分析。在两名患者中观察到至少17kb的缺失,从外显子2下游开始并延伸至基因的3'端之外。这些观察结果为我们家族中观察到的酰基辅酶A氧化酶缺乏症提供了分子基础。此外,我们的研究将有助于对疑似酰基辅酶A氧化酶疾病的无关家族中的遗传缺陷进行表征。