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跨膜结构域长度作为生物体复杂性和病毒运输机制的特征。

Transmembrane Domain Lengths Serve as Signatures of Organismal Complexity and Viral Transport Mechanisms.

作者信息

Singh Snigdha, Mittal Aditya

机构信息

Kusuma School of Biological Sciences, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.

出版信息

Sci Rep. 2016 Mar 1;6:22352. doi: 10.1038/srep22352.

DOI:10.1038/srep22352
PMID:26925972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4772119/
Abstract

It is known that membrane proteins are important in various secretory pathways, with a possible role of their transmembrane domains (TMDs) as sorting determinant factors. One key aspect of TMDs associated with various "checkposts" (i.e. organelles) of intracellular trafficking is their length. To explore possible linkages in organisms with varying "complexity" and differences in TMD lengths of membrane proteins associated with different organelles (such as Endoplasmic Reticulum, Golgi, Endosomes, Nucleus, Plasma Membrane), we analyzed ~70,000 membrane protein sequences in over 300 genomes of fungi, plants, non-mammalian vertebrates and mammals. We report that as we move from simpler to complex organisms, variation in organellar TMD lengths decreases, especially compared to their respective plasma membranes, with increasing organismal complexity. This suggests an evolutionary pressure in modulating length of TMDs of membrane proteins with increasing complexity of communication between sub-cellular compartments. We also report functional applications of our findings by discovering remarkable distinctions in TMD lengths of membrane proteins associated with different intracellular transport pathways. Finally, we show that TMD lengths extracted from viral proteins can serve as somewhat weak indicators of viral replication sites in plant cells but very strong indicators of different entry pathways employed by animal viruses.

摘要

众所周知,膜蛋白在各种分泌途径中很重要,其跨膜结构域(TMDs)可能作为分选决定因素发挥作用。与细胞内运输的各种“检查站”(即细胞器)相关的TMDs的一个关键方面是它们的长度。为了探索不同“复杂程度”的生物体中可能存在的联系,以及与不同细胞器(如内质网、高尔基体、内体、细胞核、质膜)相关的膜蛋白TMD长度的差异,我们分析了真菌、植物、非哺乳动物脊椎动物和哺乳动物300多个基因组中的约7万个膜蛋白序列。我们报告,随着我们从简单生物体向复杂生物体转变,细胞器TMD长度的变化会减少,尤其是与它们各自的质膜相比,随着生物体复杂性的增加。这表明,随着亚细胞区室之间通讯复杂性的增加,在调节膜蛋白TMD长度方面存在进化压力。我们还通过发现与不同细胞内运输途径相关的膜蛋白TMD长度的显著差异,报告了我们研究结果的功能应用。最后,我们表明,从病毒蛋白中提取的TMD长度可以作为植物细胞中病毒复制位点的较弱指标,但可以作为动物病毒采用的不同进入途径的非常强的指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/91072fe36781/srep22352-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/7a4eb05b2ac1/srep22352-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/d8f9fa2c02e5/srep22352-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/24fd3ba04892/srep22352-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/456b32f456ab/srep22352-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/be74f64a4312/srep22352-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/b23431fe35f7/srep22352-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/91072fe36781/srep22352-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/7a4eb05b2ac1/srep22352-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/d8f9fa2c02e5/srep22352-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/24fd3ba04892/srep22352-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/456b32f456ab/srep22352-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/be74f64a4312/srep22352-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/b23431fe35f7/srep22352-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f2/4772119/91072fe36781/srep22352-f7.jpg

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