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UDP-糖基转移酶基因在分生组织中的定位诱导表达对豌豆和苜蓿的生长发育至关重要。

Meristem-localized inducible expression of a UDP-glycosyltransferase gene is essential for growth and development in pea and alfalfa.

作者信息

Woo H H, Orbach M J, Hirsch A M, Hawes M C

机构信息

Department of Plant Pathology, University of Arizona, Tucson, Arizona 85721, USA.

出版信息

Plant Cell. 1999 Dec;11(12):2303-15. doi: 10.1105/tpc.11.12.2303.

Abstract

PsUGT1, which encodes a microsomal UDP-glucuronosyltransferase, was cloned from root tips of Pisum sativum. PsUGT1 expression is correlated with mitosis and strongly induced in dividing cells. A region at the C terminus of the encoded protein is closely related to the UDP-glucuronic acid binding site consensus sequence, and the protein encoded by PsUGT1 catalyzes conjugation of UDP-glucuronic acid to an unknown compound. Overexpression of PsUGT1 sense mRNA has no detectable effect on transgenic pea hairy root cultures or regenerated alfalfa. However, inhibiting PsUGT1 expression by the constitutive expression of antisense mRNA (under the control of the cauliflower mosaic virus 35S promoter) markedly retards growth and development of transgenic alfalfa. Cell structure and organization in the antisense plants are similar to those of controls, but plant growth is reduced and development is delayed. This inhibition in growth is correlated with a twofold delay in the time required for completion of a cell cycle and with a >99% inhibition of border cell production. Inhibition of PsUGT1 expression by meristem-localized inducible expression of PsUGT1 antisense mRNA (under the control of its own promoter) is lethal both in pea hairy roots and in transgenic alfalfa plants. These results indicate that PsUGT1 expression is required for normal plant growth and development, and they are consistent with the hypothesis that this UDP-glycosyltransferase regulates activity of a ligand(s) needed for cell division.

摘要

PsUGT1编码一种微粒体UDP-葡萄糖醛酸基转移酶,它是从豌豆根尖中克隆出来的。PsUGT1的表达与有丝分裂相关,并且在分裂细胞中强烈诱导表达。编码蛋白C末端的一个区域与UDP-葡萄糖醛酸结合位点共有序列密切相关,PsUGT1编码的蛋白催化UDP-葡萄糖醛酸与一种未知化合物的结合。PsUGT1正义mRNA的过表达对转基因豌豆毛状根培养物或再生苜蓿没有可检测到的影响。然而,通过组成型表达反义mRNA(在花椰菜花叶病毒35S启动子的控制下)抑制PsUGT1的表达,会显著延缓转基因苜蓿的生长和发育。反义植株的细胞结构和组织与对照相似,但植株生长减缓且发育延迟。这种生长抑制与细胞周期完成所需时间延长两倍以及边缘细胞产生受到>99%的抑制相关。通过分生组织定位的可诱导表达PsUGT1反义mRNA(在其自身启动子的控制下)抑制PsUGT1的表达,对豌豆毛状根和转基因苜蓿植株都是致死的。这些结果表明,PsUGT1的表达是植物正常生长和发育所必需的,并且与这种UDP-糖基转移酶调节细胞分裂所需配体活性的假设一致。

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