Kretz K A, Cripe D, Carson G S, Fukushima H, O'Brien J S
Department of Neurosciences, University of California, San Diego, School of Medicine, La Jolla 92093.
Genomics. 1992 Feb;12(2):276-80. doi: 10.1016/0888-7543(92)90374-2.
Fucosidosis is a rare lysosomal storage disease resulting from a nearly complete deficiency of alpha-L-fucosidase enzyme activity. Previously, cDNA encoding human fucosidase was cloned and sequenced. Here we report the determination of the human fucosidase gene structure and sequence as well as the sequence of the fucosidase pseudogene. The gene encoding fucosidase is composed of eight exons spanning 23 kb of DNA. Analysis of the sequence 5' of the open reading frame indicates the presence of multiple transcription factor binding sites but no TATA box. Northern blot analysis has confirmed an mRNA size of 2.3 kb in human lymphoblasts, testis, and epithelial cells. We have also sequenced the processed pseudogene of fucosidase. The sequence of the pseudogene is 80% identical to that of fucosidase cDNA but does not contain an open reading frame.
岩藻糖苷贮积症是一种罕见的溶酶体贮积病,由α-L-岩藻糖苷酶活性几乎完全缺乏所致。此前,编码人岩藻糖苷酶的cDNA已被克隆和测序。在此我们报告人岩藻糖苷酶基因结构和序列以及岩藻糖苷酶假基因序列的测定结果。编码岩藻糖苷酶的基因由八个外显子组成,跨越23kb的DNA。对开放阅读框5'端序列的分析表明存在多个转录因子结合位点,但没有TATA框。Northern印迹分析已证实人淋巴母细胞、睾丸和上皮细胞中mRNA大小为2.3kb。我们还对岩藻糖苷酶的加工假基因进行了测序。该假基因的序列与岩藻糖苷酶cDNA的序列80%相同,但不包含开放阅读框。