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兼性C4植物黑藻中C4响应基因的鉴定。

Identification of C4 responsive genes in the facultative C4 plant Hydrilla verticillata.

作者信息

Rao Srinath K, Fukayama Hiroshi, Reiskind Julia B, Miyao Mitsue, Bowes George

机构信息

Department of Botany, University of Florida, Gainesville, FL 32611-8526, USA.

出版信息

Photosynth Res. 2006 May;88(2):173-83. doi: 10.1007/s11120-006-9049-9. Epub 2006 Apr 19.

Abstract

The aquatic monocot Hydrilla verticillata (L.f.) Royle is a well-documented facultative C4 NADP-malic enzyme species in which the C4 and Calvin cycles operate in the same cell with the specific carboxylases confined to the cytosol and chloroplast, respectively. Several key components had already been characterized at the molecular level, thus the purpose of this study was to begin to identify other, less obvious, elements that may be necessary for a functional single-cell C4 system. Using differential display, mRNA populations from C3 and C4 H. verticillata leaves were screened and expression profiles compared. From this study, 65 clones were isolated and subjected to a customized macroarray analysis; 25 clones were found to be upregulated in C4 leaves. Northern and semi-quantitative RT-PCR analyses were used for confirmation. From these screenings, 13 C4 upregulated genes were identified. Among these one encoded a previously recognized C4 phosphoenolpyruvate carboxylase, and two encoded distinct pyruvate orthophosphate dikinase isoforms, new findings for H. verticillata. Genes that encode a transporter, an aminotransferase and two chaperonins were also upregulated. Twelve false positives, mostly housekeeping genes, were determined from the Northern/semi-quantitative RT-PCR analyses. Sequence data obtained in this study are listed in the dbEST database (DV216698 to DV216767). As a single-cell C4 system that lacks Kranz anatomy, a better understanding of how H. verticillata operates may facilitate the design of a transgenic C4 system in a C3 crop species.

摘要

水生单子叶植物黑藻(Hydrilla verticillata (L.f.) Royle)是一种有充分文献记载的兼性C4 NADP-苹果酸酶植物,其中C4和卡尔文循环在同一细胞中运行,特定的羧化酶分别局限于细胞质和叶绿体中。几个关键成分已经在分子水平上得到了表征,因此本研究的目的是开始鉴定其他可能对功能性单细胞C4系统必不可少但不太明显的元素。利用差异显示技术,对C3和C4黑藻叶片的mRNA群体进行筛选,并比较表达谱。通过这项研究,分离出65个克隆并进行定制的宏阵列分析;发现25个克隆在C4叶片中上调。采用Northern和半定量RT-PCR分析进行验证。通过这些筛选,鉴定出13个C4上调基因。其中一个编码先前已识别的C4磷酸烯醇式丙酮酸羧化酶,两个编码不同的丙酮酸磷酸双激酶同工型,这是黑藻的新发现。编码转运蛋白、转氨酶和两种伴侣蛋白的基因也上调。通过Northern/半定量RT-PCR分析确定了12个假阳性,主要是管家基因。本研究获得的序列数据列于dbEST数据库(DV216698至DV216767)。作为一种缺乏花环结构的单细胞C4系统,更好地了解黑藻的运作方式可能有助于在C3作物物种中设计转基因C4系统。

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