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掌控死亡:病毒 Bcl-2 在双链 DNA 病毒中的作用。

Mastering Death: The Roles of Viral Bcl-2 in dsDNA Viruses.

机构信息

Genome Sciences and Cancer Division, The John Curtin School of Medical Research, Australian National University, Canberra 2601, Australia.

Department of Biochemistry and Chemistry, La Trobe University, Melbourne, VIC 3086, Australia.

出版信息

Viruses. 2024 May 30;16(6):879. doi: 10.3390/v16060879.

Abstract

Proteins of the Bcl-2 family regulate cellular fate via multiple mechanisms including apoptosis, autophagy, senescence, metabolism, inflammation, redox homeostasis, and calcium flux. There are several regulated cell death (RCD) pathways, including apoptosis and autophagy, that use distinct molecular mechanisms to elicit the death response. However, the same proteins/genes may be deployed in multiple biochemical pathways. In apoptosis, Bcl-2 proteins control the integrity of the mitochondrial outer membrane (MOM) by regulating the formation of pores in the MOM and apoptotic cell death. A number of prosurvival genes populate the genomes of viruses including those of the pro-survival Bcl-2 family. Viral Bcl-2 proteins are sequence and structural homologs of their cellular counterparts and interact with cellular proteins in apoptotic and autophagic pathways, potentially allowing them to modulate these pathways and determine cellular fate.

摘要

Bcl-2 家族蛋白通过多种机制调节细胞命运,包括细胞凋亡、自噬、衰老、代谢、炎症、氧化还原平衡和钙流。有几种受调控的细胞死亡 (RCD) 途径,包括细胞凋亡和自噬,它们使用不同的分子机制引发死亡反应。然而,相同的蛋白质/基因可能被部署在多种生化途径中。在细胞凋亡中,Bcl-2 蛋白通过调节线粒体外膜 (MOM) 中孔的形成来控制 MOM 的完整性和细胞凋亡。许多生存基因存在于病毒的基因组中,包括生存 Bcl-2 家族的基因。病毒 Bcl-2 蛋白是其细胞对应物的序列和结构同源物,与细胞凋亡和自噬途径中的细胞蛋白相互作用,可能使它们能够调节这些途径并决定细胞命运。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9a7/11209288/18c414be94df/viruses-16-00879-g002.jpg

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