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生长素结合蛋白——抗体与基因

Auxin-binding protein--antibodies and genes.

作者信息

Lazarus C M, Napier R M, Yu L X, Lynas C, Venis M A

机构信息

Department of Botany, University of Bristol, UK.

出版信息

Symp Soc Exp Biol. 1991;45:129-48.

PMID:1668837
Abstract

Of several auxin-binding systems that have been characterised the auxin-binding protein (ABP) of maize coleoptile membranes is the best candidate for a true auxin receptor. ABP, which exists as a homodimer of 22 x 10(3) M(r) glycosylated subunits, has been purified, and monoclonal and polyclonal antibodies raised against it. Electrophysiological studies with antibodies indicated the presence of a functional population of auxin receptors on the exterior face of the plasmalemma; electrophysiological experiments with impermeant auxin analogues now reinforce this conclusion. An epitope mapping kit has been used to identify the major epitopes recognised by antibody preparations. Three major epitopes, bracketing the glycosylation site, have been identified in the polyclonal serum. They are also represented in antisera produced in other laboratories and are conserved in ABP prepared from other plants. One monoclonal antibody recognises an epitope close to the amino terminus of ABP and two others recognise the carboxy terminus. The latter antibodies have been used in a sandwich ELISA to demonstrate that auxin binding induces a conformational change in ABP. Maize ABP is encoded by a small gene family and cDNA and genomic clones have been isolated. With a single exception, predicted amino acid sequences indicate remarkably little heterogeneity. The exceptional cDNA sequence predicts 87% amino acid homology with the major class of proteins. Four introns are apparent in the sequence of a complete ABP gene; their sequences are very highly conserved in an incompletely-cloned second gene lacking the first exon. The major difference between the two genes lies in the length of the first intron, which has been estimated to exceed 5.2 kb in the incomplete gene. The site of initiation of transcription has not been unambiguously identified in the complete gene, and some evidence suggests that there may be an additional intron. Homology to maize ABP cDNA has been detected in the genomes of Arabidopsis, spinach and strawberry but not in that of tobacco. A sequence located within the 3'-half of the maize cDNA is highly repeated in the strawberry genome, from which clones with homology to both halves of the maize cDNA (i.e. putative ABP genes) have been isolated.

摘要

在已被鉴定的几种生长素结合系统中,玉米胚芽鞘膜的生长素结合蛋白(ABP)是真正生长素受体的最佳候选者。ABP以22×10³ M(r) 糖基化亚基的同型二聚体形式存在,已被纯化,并制备了针对它的单克隆抗体和多克隆抗体。用抗体进行的电生理研究表明,质膜外表面存在功能性的生长素受体群体;用非渗透性生长素类似物进行的电生理实验现在强化了这一结论。一个表位作图试剂盒已被用于鉴定抗体制剂识别的主要表位。在多克隆血清中已鉴定出三个主要表位,它们包围着糖基化位点。它们也存在于其他实验室产生的抗血清中,并且在从其他植物制备的ABP中是保守的。一种单克隆抗体识别靠近ABP氨基末端的一个表位,另外两种识别羧基末端。后一种抗体已被用于夹心ELISA中,以证明生长素结合会诱导ABP发生构象变化。玉米ABP由一个小基因家族编码,并且已分离出cDNA和基因组克隆。除了一个例外,预测的氨基酸序列显示出非常小的异质性。这个特殊的cDNA序列预测与主要类别的蛋白质有87%的氨基酸同源性。在一个完整的ABP基因序列中明显有四个内含子;它们的序列在一个缺少第一个外显子的未完全克隆的第二个基因中非常高度保守。这两个基因之间的主要差异在于第一个内含子的长度,据估计在未完全的基因中超过5.2 kb。在完整基因中尚未明确鉴定出转录起始位点,并且有一些证据表明可能还有一个额外的内含子。在拟南芥、菠菜和草莓的基因组中检测到了与玉米ABP cDNA的同源性,但在烟草的基因组中未检测到。位于玉米cDNA 3'-半部分内的一个序列在草莓基因组中高度重复,已从其中分离出与玉米cDNA两半部分都有同源性的克隆(即假定的ABP基因)。

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