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线粒体分裂与融合基因密码子使用分析的分子见解:与神经退行性疾病的相关性

Molecular insights into codon usage analysis of mitochondrial fission and fusion gene: relevance to neurodegenerative diseases.

作者信息

Khandia Rekha, Pandey Megha Katare, Garg Rajkumar, Khan Azmat Ali, Baklanov Igor, Alanazi Amer M, Nepali Prakash, Gurjar Pankaj, Choudhary Om Prakash

机构信息

Departments of Biochemistry and Genetics.

Translational Medicine Center, All India Institute of Medical Sciences, Bhopal.

出版信息

Ann Med Surg (Lond). 2024 Jan 15;86(3):1416-1425. doi: 10.1097/MS9.0000000000001725. eCollection 2024 Mar.

Abstract

Mitochondrial dysfunction is the leading cause of neurodegenerative disorders like Alzheimer's disease and Parkinson's disease. Mitochondria is a highly dynamic organelle continuously undergoing the process of fission and fusion for even distribution of components and maintaining proper shape, number, and bioenergetic functionality. A set of genes governs the process of fission and fusion. , and govern fusion, while , , , and genes control fission. Determination of specific molecular patterns of transcripts of these genes revealed the impact of compositional constraints on selecting optimal codons. AGA and CCA codons were over-represented, and CCC, GTC, TTC, GGG, ACG were under-represented in the fusion gene set. In contrast, CTG was over-represented, and GCG, CCG, and TCG were under-represented in the fission gene set. Hydropathicity analysis revealed non-polar protein products of both fission and fusion gene set transcripts. AGA codon repeats are an integral part of translational regulation machinery and present a distinct pattern of over-representation and under-representation in different transcripts within the gene sets, suggestive of selective translational force precisely controlling the occurrence of the codon. Out of six synonymous codons, five synonymous codons encoding for leucine were used differently in both gene sets. Hence, forces regulating the occurrence of AGA and five synonymous leucine-encoding codons suggest translational selection. A correlation of mutational bias with gene expression and codon bias and GRAVY and AROMA signifies the selection pressure in both gene sets, while the correlation of compositional bias with gene expression, codon bias, protein properties, and minimum free energy signifies the presence of compositional constraints. More than 25% of codons of both gene sets showed a significant difference in codon usage. The overall analysis shed light on molecular features of gene sets involved in fission and fusion.

摘要

线粒体功能障碍是阿尔茨海默病和帕金森病等神经退行性疾病的主要原因。线粒体是一种高度动态的细胞器,不断经历裂变和融合过程,以实现成分的均匀分布并维持适当的形状、数量和生物能量功能。一组基因控制着裂变和融合过程。 、 和 控制融合,而 、 、 和 基因控制裂变。对这些基因转录本的特定分子模式的测定揭示了组成限制对选择最佳密码子的影响。AGA和CCA密码子出现频率过高,而CCC、GTC、TTC、GGG、ACG在融合基因集中出现频率过低。相反,CTG在裂变基因集中出现频率过高,而GCG、CCG和TCG出现频率过低。亲水性分析揭示了裂变和融合基因集转录本的非极性蛋白质产物。AGA密码子重复是翻译调控机制的一个组成部分,并且在基因集内的不同转录本中呈现出明显的过高和过低出现频率模式,这表明存在精确控制密码子出现的选择性翻译力。在六个同义密码子中,编码亮氨酸的五个同义密码子在两个基因集中的使用方式不同。因此,调节AGA和五个编码亮氨酸的同义密码子出现的力量表明存在翻译选择。突变偏好与基因表达、密码子偏好以及GRAVY和AROMA之间的相关性表明两个基因集中都存在选择压力,而组成偏好与基因表达、密码子偏好、蛋白质特性和最小自由能之间的相关性表明存在组成限制。两个基因集超过25%的密码子在密码子使用上存在显著差异。总体分析揭示了参与裂变和融合的基因集的分子特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04bf/10923317/4abeec9449a4/ms9-86-1416-g001.jpg

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