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两个与草莓(凤梨草莓品种钱德勒)成熟相关的果胶裂解酶基因的克隆与特性分析

Cloning and characterization of two ripening-related strawberry (Fragaria x ananassa cv. Chandler) pectate lyase genes.

作者信息

Benítez-Burraco Antonio, Blanco-Portales Rosario, Redondo-Nevado José, Bellido M Luz, Moyano Enriqueta, Caballero José-L, Muñoz-Blanco Juan

机构信息

Departamento de Bioquímica y Biología Molecular, Edificio Severo Ochoa (Edificio C-6), Campus Universitario de Rabanales, Universidad de Córdoba, 14071 Córdoba, Spain.

出版信息

J Exp Bot. 2003 Feb;54(383):633-45. doi: 10.1093/jxb/erg065.

Abstract

Two genomic clones corresponding to putative pectate lyase genes (plA and plB) were isolated and characterized in strawberry (Fragaria x ananassa cv. Chandler). The corresponding ORFs for the plA and plB genes revealed deduced proteins of 451 and 439 amino acids, respectively, that differ from that of the previously isolated strawberry plC gene. Southern blot analysis has shown that while the plB gene is a single copy gene, the plA gene is probably encoded by a small multigene family. By using specific probes corresponding to the untranslated 3' terminal region of the pl genes, and QRT-PCR methodology, the spatio-temporal expression pattern of both strawberry pl genes have been compared with that of the plC gene. The three transcripts were specifically expressed only in fruit and mainly during the ripening stages. Moreover, the expression of the plA and plB genes was induced in green de-achened fruit, but this increase was reduced by the external application of auxins as was the expression of plC. The expression of both pl genes was also strongly reduced in harvested fruit kept in controlled atmosphere (CA) containing high CO(2) levels. Immunolocalization studies using antibodies raised against the strawberry PL proteins placed the proteins in the cell wall of parenchymatic cells of the fruit receptacle. The role of pl genes in cell-wall disassembly and fruit ripening softening is discussed.

摘要

在草莓(凤梨草莓品种钱德勒)中分离并鉴定了两个与假定的果胶酸裂解酶基因(plA和plB)相对应的基因组克隆。plA和plB基因的相应开放阅读框分别显示出推导的451和439个氨基酸的蛋白质,这与先前分离的草莓plC基因不同。Southern印迹分析表明,虽然plB基因是单拷贝基因,但plA基因可能由一个小的多基因家族编码。通过使用与pl基因的非翻译3'末端区域相对应的特异性探针和定量逆转录聚合酶链反应(QRT-PCR)方法,将两个草莓pl基因的时空表达模式与plC基因的进行了比较。这三种转录本仅在果实中特异性表达,且主要在成熟阶段表达。此外,plA和plB基因在绿色去瘦果的果实中被诱导表达,但这种增加被生长素的外部施用所降低,plC基因的表达也是如此。在含有高浓度二氧化碳的控制气氛(CA)中保存的收获果实中,两个pl基因的表达也强烈降低。使用针对草莓PL蛋白产生的抗体进行的免疫定位研究将这些蛋白定位在果实花托薄壁细胞的细胞壁中。本文讨论了pl基因在细胞壁分解和果实成熟软化中的作用。

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