Banning Antje, König Jan F, Gray Steven J, Tikkanen Ritva
Institute of Biochemistry, Medical Faculty, University of Giessen, Friedrichstrasse 24, 35392 Giessen, Germany.
Gene Therapy Center and Department of Ophthalmology, University of North Carolina, Chapel Hill, NC 27302, USA.
Int J Mol Sci. 2017 Mar 26;18(4):706. doi: 10.3390/ijms18040706.
Aspartylglucosaminidase (AGA) is a lysosomal hydrolase that participates in the breakdown of glycoproteins. Defects in the AGA gene result in a lysosomal storage disorder, aspartylglucosaminuria (AGU), that manifests mainly as progressive mental retardation. A number of AGU missense mutations have been identified that result in reduced AGA activity. Human variants that contain either Ser or Thr in position 149 have been described, but it is unknown if this affects AGA processing or activity. Here, we have directly compared the Ser149/Thr149 variants of AGA and show that they do not differ in terms of relative specific activity or processing. Therefore, Thr149 AGA, which is the rare variant, can be considered as a neutral or benign variant. Furthermore, we have here produced codon-optimized versions of these two variants and show that they are expressed at significantly higher levels than AGA with the natural codon-usage. Since optimal AGA expression is of vital importance for both gene therapy and enzyme replacement, our data suggest that use of codon-optimized AGA may be beneficial for these therapy options.
天冬氨酰葡糖胺酶(AGA)是一种参与糖蛋白分解的溶酶体水解酶。AGA基因缺陷会导致一种溶酶体贮积症,即天冬氨酰葡糖胺尿症(AGU),主要表现为进行性智力迟钝。已鉴定出一些导致AGA活性降低的AGU错义突变。已描述了在第149位含有丝氨酸(Ser)或苏氨酸(Thr)的人类变体,但尚不清楚这是否会影响AGA的加工或活性。在此,我们直接比较了AGA的Ser149/Thr149变体,结果表明它们在相对比活性或加工方面没有差异。因此,罕见的Thr149 AGA变体可被视为中性或良性变体。此外,我们在此制备了这两种变体的密码子优化版本,并表明它们的表达水平明显高于使用天然密码子的AGA。由于最佳的AGA表达对基因治疗和酶替代都至关重要,我们的数据表明使用密码子优化的AGA可能对这些治疗方案有益。