结构分析揭示长ssrs可能影响4Fe-4S蛋白在甲烷生成中的灵活性和功能。

IF 2.7 4区 生物学 Q2 MICROBIOLOGY
Sahil Mahfooz, Pragya Anand, Ajay Bhatia, Jitendra Narayan, Motrih Al-Mutiry, Mohd Saeed, Irfan Ahmad, Yusuf Akhter
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引用次数: 0

摘要

简单重复序列(SSRs)是生物体基因组的基本组成部分,在基因组的组织和进化中起着至关重要的作用。在这项研究中,我们研究了长SSRs在不同甲烷菌中的流行率、相对丰度(RA)和相对密度(RD),以揭示它们的进化相关性和潜在的功能意义。其中,风产甲烷球菌(Methanococcus aeolicus)的RA和RD值最高,分别为110.0和1844.5,其次是liminatans (Methanococcus liminans),分别为86.6和1087.0。相比之下,最低的是阿比西尼亚产甲烷球菌(20.6和277.0)。值得注意的是,产甲烷菌普遍以A + t丰富的基因组为特征,且SSR频率与AT含量呈正相关(r = 0.380)。SSRs在基因区和基因间分布不均匀,平均65.4个(67.4%)SSRs位于基因区,31.6个(32.4%)SSRs位于基因区。为了探索ssr的潜在功能作用,我们对马里帕洛迪甲烷球菌中含有长ssr的4Fe-4S结构域蛋白进行了三维结构建模。该模型显示,SSR插入可能影响结构域-结构域相互作用,调节活性位点的可及性和灵活性,可能有助于蛋白质在逆境条件下和甲烷生产过程中的适应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structural Insights Reveal Long-SSRs May Affect 4Fe-4S Protein Flexibility and Function in Methanogenesis.

Simple sequence repeats (SSRs) represent a fundamental component of an organism's genome and can play critical roles in genome organization and evolution. In this study, we examined the prevalence, relative abundance (RA), and relative density (RD) of long SSRs across various methanogens to uncover their evolutionary relevance and potential functional implications. Among the species analyzed, Methanococcus aeolicus exhibited the highest RA and RD values (110.0 and 1844.5, respectively), followed by Methanococcus liminatans (86.6 and 1087.0). In contrast, the lowest values were observed in Methanococcus abyssi (20.6 and 277.0). Notably, methanogens are generally characterized by A + T-rich genomes, and a positive correlation (r = 0.380) was found between SSR frequency and AT content. SSRs were distributed unevenly between genic and intergenic regions: on average, 65.4 SSRs (67.4% of total) were located in genic regions, while 31.6 SSRs (32.4%) occurred in intergenic regions. To explore potential functional effects of SSRs, we performed 3D structural modelling of a long-SSR-containing 4Fe-4S domain protein from Methanococcus maripaludis. The model revealed that SSR insertions may influence domain-domain interactions and modulate the accessibility and flexibility of the active site, potentially contributing to protein adaptation under stress conditions and during methane production.

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来源期刊
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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