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Expression, Localization and Function of a cis-Prenyltransferase in the Tapetum and Microspores of Lily Anthers

机译:顺式-戊基转移酶在百合花药的绒毡层和小孢子中的表达,定位和功能

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摘要

The cis-prenyltransferase gene LLA66 (Lilium longiflorum anther-66), the first prenyltransferase to be identified in the tapetum and microspores, was selected from a suppression subtractive cDNA library during microspore development in the anther of L. longiflorum. The LLA66 cDNA encodes a polypeptide of 308 amino acids with a calculated molecular mass of 35.7 kDa. Thermal asymmetric interlaced-PCR was employed to obtain the 5′-regulatory region of LLA66. Sequence alignment revealed that the LLA66 protein shares 30–41% identity with cis-prenyltransferases of various broad-spectrum species and is phylogenetically distinct from other monocot cis-prenyltransferases. Based on critical regulatory domains in cis-prenyltransferase, LLA66 was concluded to catalyze the production of long-chain polyprenyl products. RNA blot analysis indicated that the LLA66 gene is anther specific and differentially expressed during microspore development in the anther. In situ hybridization with the digoxigenin-labeled antisense riboprobe of LLA66 showed strong signals at the tapetal layer of the anther wall. The LLA66 mRNA was also coordinately detected in the microspores. Furthermore, gibberellin inhibitor analysis indicated that the LLA66 gene is endogenously induced by gibberellin, but its induction is independent of ethylene regulation. Reverse transcription–PCR analysis indicated that gene expression of LLA66 both in the microspore and in the anther wall increased to the maximum level, at which stage the tapetum became highly active and secretory. The enzyme activity of prenyltransferases in various stages of microspore development correlated with tapetal growth and disintegration. LLA66 was introduced into Saccharomyces cerevisiae, and the His-tagged LLA66 protein was affinity purified using Ni2+–nitrilotriacetic acid–agarose. The involvement of cis-prenyltransferase in the anther in the synthesis of dolichols and polyprenols is discussed.
机译:顺式异戊二烯转移酶基因LLA66(百合花药百合花药66)是在绒毡层和小孢子中被鉴定出的第一个异戊烯基转移酶,是从抑制作用的cDNA文库中选出的。 LLA66 cDNA编码308个氨基酸的多肽,计算的分子量为35.7 kDa。使用热不对称隔行PCR获得LLA66的5'调节区。序列比对显示,LLA66蛋白与各种广谱物种的顺式异戊二烯基转移酶具有30-41%的同一性,并且在系统发育上不同于其他单子叶植物的顺式异戊二烯基转移酶。基于顺式异戊二烯基转移酶中的关键调控域,LLA66可以催化长链聚异戊二烯基产物的产生。 RNA印迹分析表明,LLA66基因是花药特异性的,在花药中的小孢子发育过程中差异表达。与洋地黄毒苷标记的LLA66反义核糖探针的原位杂交在花药壁的绒毛层显示出强信号。在小孢子中也协同检测到LLA66 mRNA。此外,赤霉素抑制剂分析表明LLA66基因是由赤霉素内源性诱导的,但其诱导与乙烯调节无关。逆转录-PCR分析表明,LLA66在小孢子和花药壁中的基因表达均增加到最大水平,在此阶段绒毡层变得高度活跃和分泌。异戊二烯基转移酶在小孢子发育各个阶段的酶活性与绒毛生长和崩解有关。将LLA66引入酿酒酵母中,并用Ni 2 + -亚硝酸三乙酸-琼脂糖亲和纯化带有His标签的LLA66蛋白。讨论了顺式异戊二烯基转移酶在花药中参与多元醇和聚戊二烯醇的合成。

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