Programmed cell death in plants: lessons from bacteria?

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2013-03-01 Epub Date: 2012-10-16 DOI:10.1016/j.tplants.2012.09.004
Junhui Wang, Kenneth W Bayles
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引用次数: 49

Abstract

Programmed cell death (PCD) has well-established roles in the development and physiology of animals, plants, and fungi. Although aspects of PCD control appear evolutionarily conserved between these organisms, the extent of conservation remains controversial. Recently, a putative bacterial PCD protein homolog in plants was found to play a significant role in cell death control, indicating a conservation of function between these highly divergent organisms. Interestingly, these bacterial proteins are thought to be evolutionarily linked to the Bcl-2 family of proteins. In this opinion article, we propose a new unifying model to describe the relationship between bacterial and plant PCD systems and propose that the underlying control of PCD is conserved across at least three Kingdoms of life.

植物细胞程序性死亡:细菌的教训?
程序性细胞死亡(PCD)在动物、植物和真菌的发育和生理中起着重要的作用。尽管PCD控制的各个方面在这些生物之间似乎是进化保守的,但保护的程度仍然存在争议。最近,在植物中发现了一种假定的细菌PCD蛋白同源物,在细胞死亡控制中起着重要作用,表明这些高度分化的生物之间存在功能守恒。有趣的是,这些细菌蛋白被认为在进化上与Bcl-2蛋白家族有关。在这篇观点文章中,我们提出了一个新的统一模型来描述细菌和植物PCD系统之间的关系,并提出PCD的潜在控制至少在三个生命王国中是保守的。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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