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马铃薯质体编码的羧基转移酶亚基(accD)基因的特性分析

Characterization of the plastid-encoded carboxyltransferase subunit (accD) gene of potato.

作者信息

Lee Sang Sook, Jeong Won Joong, Bae Jung Myung, Bang Jae Wook, Liu Jang Ryol, Harn Chee Hark

机构信息

Plant Cell and Molecular Biology Research Unit, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Korea.

出版信息

Mol Cells. 2004 Jun 30;17(3):422-9.

Abstract

The plastid accD gene encoding the carboxyltransferase b subunit of acetyl-coenzyme A carboxylase (ACCase) was cloned from potato. Potato accD (saccD) is 2487 bp in length with a 614 bp 5 cent upstream promoter region and an ORF of 1524 bp, corresponding to a polypeptide of 507 amino acids. The N-terminal region lacks recognizable motifs, while the C-terminal regions contains five motifs. Among these is motif II, PLIIVCASGGARMQE, the sole motif present in all available accD sequences of plants and animals, and of E. coli, suggesting that this motif may correspond to the catalytic site. saccD has the typical prokaryotic promoter signatures, TTGACA and TATCAA, which are -35 and -10-like sequences for plastid-encoded RNA polymerase (PEP), at positions -184 and -160, respectively. However, it seems to be transcribed by the nucleus-encoded RNA polymerase because it is expressed in tuber and root, and in the dark (under crippled PEP conditions) and its transcription initiation sites do not correspond to those of PEP. saccD is expressed in all potato tissues, i.e., leaf, stem, root, and tuber, and its transcript is produced at a similar rate in the light and dark, at different developmental stages, and during growth in the presence of different sugars and carbon sources. Taken together, our results suggest that potato accD is a housekeeping gene constitutively expressed in both chloroplast and amyloplast.

摘要

从马铃薯中克隆了编码乙酰辅酶A羧化酶(ACCase)羧基转移酶b亚基的质体accD基因。马铃薯accD(saccD)全长2487 bp,有一个614 bp的5′上游启动子区域和一个1524 bp的开放阅读框,对应一个507个氨基酸的多肽。N端区域缺乏可识别的基序,而C端区域包含五个基序。其中基序II,PLIIVCASGGARMQE,是植物、动物和大肠杆菌所有可用accD序列中唯一存在的基序,表明该基序可能对应催化位点。saccD具有典型的原核启动子特征,TTGACA和TATCAA,分别位于-184和-160位置,是质体编码RNA聚合酶(PEP)的-35和-10样序列。然而,它似乎是由核编码的RNA聚合酶转录的,因为它在块茎和根中表达,在黑暗中(在PEP功能受损的条件下)表达,并且其转录起始位点与PEP的不同。saccD在马铃薯所有组织中表达,即叶、茎、根和块茎,并且在不同发育阶段、在不同糖类和碳源存在下生长时,其转录本在光照和黑暗条件下以相似的速率产生。综上所述,我们的结果表明马铃薯accD是一个在叶绿体和造粉体中组成型表达的管家基因。

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