Allison L A
Department of Biochemistry, University of Nebraska, NE 68588-0664, Lincoln, USA.
Biochimie. 2000 Jun-Jul;82(6-7):537-48. doi: 10.1016/s0300-9084(00)00611-8.
Expression of plastid genes is controlled at both transcriptional and post-transcriptional levels in response to developmental and environmental signals. In many cases this regulation is mediated by nuclear-encoded proteins acting in concert with the endogenous plastid gene expression machinery. Transcription in plastids is accomplished by two distinct RNA polymerase enzymes, one of which resembles eubacterial RNA polymerases in both subunit structure and promoter recognition properties. The holoenzyme contains a catalytic core composed of plastid-encoded subunits, assembled with a nuclear-encoded promoter-specificity factor, sigma. Based on examples of transcriptional regulation in bacteria, it is proposed that differential activation of sigma factors may provide the nucleus with a mechanism to control expression of groups of plastid genes. Hence, much effort has focused on identifying and characterizing sigma-like factors in plants. While fractionation studies had identified several candidate sigma factors in purified RNA polymerase preparations, it was only 4 years ago that the first sigma factor genes were cloned from two photosynthetic eukaryotes, both of which were red algae. More recently this achievement has extended to the identification of families of sigma-like factor genes from several species of vascular plants. Now, efforts in the field are directed at understanding the roles in plastid transcription of each member of the rapidly expanding plant sigma factor gene family. Recent results suggest that accumulation of individual sigma-like factors is controlled by light, by plastid type and/or by a particular stage of chloroplast development. These data mesh nicely with accumulating evidence that the core sigma-binding regions of plastid promoters mediate regulated transcription in response to light-regime and plastid type or developmental state. In this review I will outline progress made to date in identifying and characterizing the sigma-like factors of plants, and in dissecting their potential roles in chloroplast gene expression.
质体基因的表达在转录和转录后水平上受到调控,以响应发育和环境信号。在许多情况下,这种调控是由核编码蛋白与内源性质体基因表达机制协同作用介导的。质体中的转录由两种不同的RNA聚合酶完成,其中一种在亚基结构和启动子识别特性上都类似于真细菌RNA聚合酶。全酶包含一个由质体编码亚基组成的催化核心,与一个核编码的启动子特异性因子sigma组装在一起。基于细菌转录调控的例子,有人提出sigma因子的差异激活可能为细胞核提供一种控制质体基因组表达的机制。因此,许多努力都集中在鉴定和表征植物中的类sigma因子上。虽然分级分离研究在纯化的RNA聚合酶制剂中鉴定出了几个候选sigma因子,但直到4年前才从两种光合真核生物中克隆出第一个sigma因子基因,这两种生物都是红藻。最近,这一成果已扩展到从几种维管植物中鉴定类sigma因子基因家族。现在,该领域的努力方向是了解迅速扩大的植物sigma因子基因家族中每个成员在质体转录中的作用。最近的结果表明,单个类sigma因子的积累受光、质体类型和/或叶绿体发育的特定阶段控制。这些数据与越来越多的证据非常吻合,即质体启动子的核心sigma结合区域介导对光照条件、质体类型或发育状态的响应的调控转录。在这篇综述中,我将概述迄今为止在鉴定和表征植物类sigma因子以及剖析它们在叶绿体基因表达中的潜在作用方面所取得的进展。