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一个未翻译的顺式元件调控白花菜叶肉细胞中多种C4酶的积累。

An Untranslated cis-Element Regulates the Accumulation of Multiple C4 Enzymes in Gynandropsis gynandra Mesophyll Cells.

作者信息

Williams Ben P, Burgess Steven J, Reyna-Llorens Ivan, Knerova Jana, Aubry Sylvain, Stanley Susan, Hibberd Julian M

机构信息

Department of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom.

Department of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom

出版信息

Plant Cell. 2016 Feb;28(2):454-65. doi: 10.1105/tpc.15.00570. Epub 2016 Jan 15.

Abstract

C4 photosynthesis is a complex phenotype that allows more efficient carbon capture than the ancestral C3 pathway. In leaves of C4 species, hundreds of transcripts increase in abundance compared with C3 relatives and become restricted to mesophyll (M) or bundle sheath (BS) cells. However, no mechanism has been reported that regulates the compartmentation of multiple enzymes in M or BS cells. We examined mechanisms regulating CARBONIC ANHYDRASE4 (CA4) in C4 Gynandropsis gynandra. Increased abundance is directed by both the promoter region and introns of the G. gynandra gene. A nine-nucleotide motif located in the 5' untranslated region (UTR) is required for preferential accumulation of GUS in M cells. This element is present and functional in three additional 5' UTRs and six 3' UTRs where it determines accumulation of two isoforms of CA and pyruvate,orthophosphate dikinase in M cells. Although the GgCA4 5' UTR is sufficient to direct GUS accumulation in M cells, transcripts encoding GUS are abundant in both M and BS. Mutating the GgCA4 5' UTR abolishes enrichment of protein in M cells without affecting transcript abundance. The work identifies a mechanism that directs cell-preferential accumulation of multiple enzymes required for C4 photosynthesis.

摘要

C4光合作用是一种复杂的表型,它比祖先的C3途径能更有效地捕获碳。在C4植物物种的叶片中,与C3亲缘植物相比,数百种转录本的丰度增加,并局限于叶肉(M)细胞或维管束鞘(BS)细胞。然而,尚未有报道称存在调节M或BS细胞中多种酶区室化的机制。我们研究了C4植物白花菜中碳酸酐酶4(CA4)的调节机制。白花菜基因的启动子区域和内含子均能导致CA4丰度增加。位于5'非翻译区(UTR)的一个九核苷酸基序是GUS在M细胞中优先积累所必需的。该元件在另外三个5'UTR和六个3'UTR中存在且具有功能,它决定了CA的两种同工型和丙酮酸磷酸双激酶在M细胞中的积累。尽管GgCA4的5'UTR足以指导GUS在M细胞中的积累,但编码GUS的转录本在M和BS细胞中均很丰富。突变GgCA4的5'UTR会消除M细胞中蛋白质的富集,而不影响转录本丰度。这项研究确定了一种指导C4光合作用所需多种酶在细胞中优先积累的机制。

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