Computational Chemistry Group, Computational Engineering and Networking, AMRITA Vishwa Vidyapeetham, Amritanagar, Coimbatore, India.
Funct Integr Genomics. 2011 Dec;11(4):519-22. doi: 10.1007/s10142-011-0238-z. Epub 2011 Jul 19.
The ApoE gene responsible for the Alzheimer's disease has been examined to identify functional consequences of single-nucleotide polymorphisms (SNPs). Eighty-eight SNPs have been identified in the ApoE gene in which 31 are found to be nonsynonymous, 8 of them are coding synonymous, 33 are found to be in intron, and 3 are in untranslated region. The SNPs found in the untranslated region consisted of two SNPs from 5' and one SNP from the 3'. Twenty-nine percent of the identified nsSNPs have been reported as damaging. In the analysis of SNPs in the UTR regions, it has been recognized that rs72654467 from 5' and rs71673244 from 5' and 3' are responsible for the alteration in levels of expression. Both native and mutant protein structures were analyzed along with the stabilization residues. It has been concluded that among all SNPs of ApoE, the mutation in rs11542041 (R132S) has the most significant effect on functional variation.
负责阿尔茨海默病的 ApoE 基因已被检测,以确定单核苷酸多态性 (SNP) 的功能后果。在 ApoE 基因中已鉴定出 88 个 SNP,其中 31 个是非同义 SNP,其中 8 个是编码同义 SNP,33 个位于内含子中,3 个位于非翻译区。非翻译区中的 SNP 由 5'的两个 SNP 和 3'的一个 SNP 组成。已鉴定出的 nsSNP 中有 29%被报告为有害。在对 UTR 区域中的 SNP 进行分析时,已认识到 5'的 rs72654467 和 5'和 3'的 rs71673244 负责改变表达水平。对天然和突变蛋白结构进行了分析,并确定了稳定残基。结论是,在 ApoE 的所有 SNP 中,rs11542041(R132S)的突变对功能变异的影响最大。