Plant A L, Cohen A, Moses M S, Bray E A
Department of Botany and Plant Sciences, University of California, Riverside, California 92521-0124.
Plant Physiol. 1991 Nov;97(3):900-6. doi: 10.1104/pp.97.3.900.
The nucleotide sequence of le16, a tomato (Lycopersicon esculentum Mill.) gene induced by drought stress and regulated by abscisic acid specifically in aerial vegetative tissue, is presented. The single open reading frame contained within the gene has the capacity to encode a polypeptide of 12.7 kilodaltons and is interrupted by a small intron. The predicted polypeptide is rich in leucine, glycine, and alanine and has an isoelectric point of 8.7. The amino terminus is hydrophobic and characteristic of signal sequences that target polypeptides for export from the cytoplasm. There is homology (47.2% identity) between the amino terminus of the LE 16 polypeptide and the corresponding amino terminal domain of the maize phospholipid transfer protein. le16 was expressed in drought-stressed leaf, petiole, and stem tissue and to a much lower extent in the pericarp of mature green tomato fruit and developing seeds. No expression was detected in the pericarp of red fruit or in drought-stressed roots. Expression of le16 was also induced in leaf tissue by a variety of other abiotic stresses including polyethylene glycol-mediated water deficit, salinity, cold stress, and heat stress. None of these stresses or direct applications of abscisic acid induced the expression of le16 in the roots of the same plants. The unique expression characteristics of this gene indicates that novel regulatory mechanisms, in addition to endogenous abscisic acid, are involved in controlling gene expression.
本文介绍了番茄(Lycopersicon esculentum Mill.)中一个受干旱胁迫诱导、由脱落酸特异性调控于地上营养组织中的基因le16的核苷酸序列。该基因包含的单一开放阅读框能够编码一个12.7千道尔顿的多肽,并被一个小内含子打断。预测的多肽富含亮氨酸、甘氨酸和丙氨酸,等电点为8.7。氨基末端具有疏水性,是将多肽输出细胞质的信号序列的特征。LE 16多肽的氨基末端与玉米磷脂转移蛋白的相应氨基末端结构域之间存在同源性(47.2%的同一性)。le16在干旱胁迫的叶片、叶柄和茎组织中表达,在成熟绿色番茄果实的果皮和发育中的种子中表达程度低得多。在红色果实的果皮或干旱胁迫的根中未检测到表达。le16的表达也可由多种其他非生物胁迫诱导,包括聚乙二醇介导的水分亏缺、盐度、冷胁迫和热胁迫,在同一植株的根中,这些胁迫或脱落酸的直接施用均未诱导le16的表达。该基因独特的表达特性表明,除了内源性脱落酸外,新的调控机制也参与了基因表达的控制。