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SIRT7的七个方面。

The seven faces of SIRT7.

作者信息

Blank Maximilian F, Grummt Ingrid

机构信息

a Molecular Biology of the Cell II , German Cancer Research Center (DKFZ), DKFZ-ZMBH Alliance , Heidelberg , Germany.

出版信息

Transcription. 2017 Mar 15;8(2):67-74. doi: 10.1080/21541264.2016.1276658. Epub 2017 Jan 9.

DOI:10.1080/21541264.2016.1276658
PMID:28067587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5423475/
Abstract

SIRT7, a member of the sirtuin family of NAD-dependent protein deacetylases, is a key mediator of many cellular activities. SIRT7 expression is linked to cell proliferation and oncogenic activity, connecting SIRT7-dependent regulation of ribosome biogenesis with checkpoints controlling cell cycle progression, metabolic homeostasis, stress resistance, aging and tumorigenesis. Despite this important functional link, the enzymatic activity, the molecular targets and physiological functions of SIRT7 are poorly defined. Here, we review recent progress in SIRT7 research and elaborate the main pathways in which SIRT7 participates.

摘要

SIRT7是烟酰胺腺嘌呤二核苷酸(NAD)依赖性蛋白质脱乙酰酶家族sirtuin的成员之一,是许多细胞活动的关键调节因子。SIRT7的表达与细胞增殖和致癌活性相关,将核糖体生物合成的SIRT7依赖性调节与控制细胞周期进程、代谢稳态、应激抗性、衰老和肿瘤发生的检查点联系起来。尽管存在这种重要的功能联系,但SIRT7的酶活性、分子靶点和生理功能仍不清楚。在此,我们综述了SIRT7研究的最新进展,并阐述了SIRT7参与的主要途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e387/5423475/f83b3a9885d0/ktrn-08-02-1276658-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e387/5423475/b29155c43416/ktrn-08-02-1276658-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e387/5423475/49196d31d198/ktrn-08-02-1276658-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e387/5423475/f83b3a9885d0/ktrn-08-02-1276658-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e387/5423475/b29155c43416/ktrn-08-02-1276658-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e387/5423475/49196d31d198/ktrn-08-02-1276658-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e387/5423475/f83b3a9885d0/ktrn-08-02-1276658-g003.jpg

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Wnt5a Signals through DVL1 to Repress Ribosomal DNA Transcription by RNA Polymerase I.Wnt5a通过DVL1发出信号,抑制RNA聚合酶I对核糖体DNA的转录。
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SIRT7 promotes lung cancer progression by destabilizing the tumor suppressor ARF.SIRT7通过使肿瘤抑制因子ARF不稳定来促进肺癌进展。
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