Laboratory of Genomics and Human Genetics, 1 Place Louis Pasteur, Institut Pasteur du Maroc, Casablanca, Morocco.
Laboratory of Physiopathology, Molecular Genetics and Biotechnology, Department of Biology, Faculty of Sciences Ain Chock, Hassan II University, Casablanca, Morocco.
Biomed Res Int. 2022 Mar 18;2022:1664825. doi: 10.1155/2022/1664825. eCollection 2022.
Meiotic chromosomes endure rapid prophase movements that ease the formation of interhomologue recombination intermediates that drive synapsis, crossing over, and segregation process. To generate these fast moves, the meiotic telomere complex (MTC) enables telomere-inner nuclear membrane attachment during meiotic prophase I and transfers cytoskeletal signals via another complex: the LINC complex. Furthermore, disruption or mutations of any of the MTC genes (TERB1, TERB2, and MAJIN) alters telomere association with the nuclear envelope leading to impairment of homologous pairing and synapsis, a meiotic arrest, and consequently to male infertility. To decipher the effect of TERB1, TERB2, and MAJIN missense mutations on protein structure, stability, and function, different bioinformatic tools were used in this study including VEP, Mutabind2, Haddock, Prodigy, Ligplot, ConSurf, DUET and MusiteDeep. In total, thirty mutations were predicted to be deleterious using VEP web server: seventeen for TERB1, eleven for TERB2, and two for MAJIN. All these single nucleotide polymorphisms were further analyzed and only 11 SNPs (W8R, G25R, P649A, I624T, C618R, F607V, S604G, C592Y, C592R, G187W, and R53C) were found to be the most damaging by at least six software tools and exert deleterious effect on the TERB1, TERB2, and MAJIN protein structures and likely functions. They revealed high conservation, less stability, and having a role in posttranslational modifications. This in silico approach provides information to gain further insights about variants that might affect stability, change binding affinity, and edit protein-protein interactions to facilitate their identification and functional characterization associated with male infertility.
减数分裂染色体经历快速的前期运动,这有助于形成同源重组中间体,从而驱动联会、交叉和分离过程。为了产生这些快速运动,减数分裂端粒复合物(MTC)使端粒与核膜在减数分裂前期 I 期间内附着,并通过另一个复合物:LINC 复合物传递细胞骨架信号。此外,任何 MTC 基因(TERB1、TERB2 和 MAJIN)的破坏或突变都会改变端粒与核膜的关联,导致同源配对和联会受损、减数分裂停滞,并最终导致男性不育。为了解释 TERB1、TERB2 和 MAJIN 错义突变对蛋白质结构、稳定性和功能的影响,本研究使用了不同的生物信息学工具,包括 VEP、Mutabind2、Haddock、Prodigy、Ligplot、ConSurf、DUET 和 MusiteDeep。总共预测到 30 个突变是有害的,其中 17 个是 TERB1 的,11 个是 TERB2 的,2 个是 MAJIN 的。所有这些单核苷酸多态性进一步进行了分析,只有 11 个 SNP(W8R、G25R、P649A、I624T、C618R、F607V、S604G、C592Y、C592R、G187W 和 R53C)被至少六个软件工具认为是最具破坏性的,对 TERB1、TERB2 和 MAJIN 蛋白质结构和功能有潜在的有害影响。它们显示出高度保守性、较低的稳定性,并在后翻译修饰中起作用。这种计算方法提供了信息,以进一步了解可能影响稳定性、改变结合亲和力并编辑蛋白质-蛋白质相互作用的变体,从而促进它们的鉴定和与男性不育相关的功能特征。