Vertebrate Arylsulfatase K (ARSK): Comparative and Evolutionary Studies of the Lysosomal 2-Sulfoglucuronate Sulfatase

R. Holmes
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Abstract

Arylsulfatase K (ARSK) is one of 17 sulfatase gene family members encoded on the human genome for which a role has been recently identified as a lysosomal 2-sulfoglucuronate sulfatase. Vertebrate ARSK sequences shared 60-82% identity but only <27% identities with other arylsulfatase family members. Comparative enzyme structures were studied, including residues with predicted roles in forming N-glycosylation sites, Ca2+ binding and active site residues. Vertebrate ARSK genes usually contained 8 coding exons. A human ARSK gene promoter comprised CpG61 and multiple TFBS, which may be involved in signal transduction, transcription activation or regulating entry into cell division. Phylogenetic analyses examined evolutionary changes for the vertebrate ARSK and the invertebrate SUL1 genes. In summary, a major role for this enzyme as a 2-sulfoglucuronate sulfatase is supported which has been conserved throughout vertebrate evolution.
脊椎动物芳基硫酸酯酶K (ARSK):溶酶体2-硫脲酸酯硫酸酯酶的比较和进化研究
Arylsulfatase K (ARSK)是人类基因组编码的17个硫酸盐酶基因家族成员之一,其作用最近被确定为溶酶体2-硫脲酸盐硫酸盐酶。脊椎动物ARSK序列与其他芳基磺化酶家族成员具有60-82%的同源性,但同源性仅<27%。研究了比较酶的结构,包括在形成n -糖基化位点、Ca2+结合位点和活性位点残基中具有预测作用的残基。脊椎动物的ARSK基因通常包含8个编码外显子。人类ARSK基因启动子由CpG61和多个TFBS组成,可能参与信号转导、转录激活或调节进入细胞分裂。系统发育分析检查了脊椎动物ARSK和无脊椎动物SUL1基因的进化变化。总之,该酶作为2-硫脲酸盐硫酸酯酶的主要作用在整个脊椎动物进化过程中得到了支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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