...
首页> 外文期刊>Botanical Studies >Expression and localization of two anther-specific genes in the tapetum and microspore of Lilium longiflorum.
【24h】

Expression and localization of two anther-specific genes in the tapetum and microspore of Lilium longiflorum.

机译:长花百合的绒毡层和小孢子中两个花药特异性基因的表达和定位。

获取原文
获取原文并翻译 | 示例
           

摘要

Two stage-specific genes have been isolated from a subtractive cDNA library constructed from developing anthers of Lilium longiflorum. Tandem 5'- and 3'-rapid amplifications of cDNA ends with polymerase chain reaction (5'- and 3'-RACE-PCR) were used to obtain the full length cDNA sequences. The LLA-89 cDNA contained an open reading frame of 303 bp encoding an acidic polypeptide of 100 amino acids with a calculated molecular mass of 10.2 kDa. The LLA-142 cDNA contained an open reading frame of 171 bp encoding a basic polypeptide of 56 amino acids with a calculated molecular mass of 5.7 kDa. The protein encoded by LLA-89 had a strong hydrophobic region at the N-terminus, indicating the presence of a signal peptide (not found in the LLA-142 protein). Sequence alignment revealed that the protein encoded by LLA-142 is novel, while the protein encoded by LLA-89 is identical to a reported LIM4 protein with unknown function. Total RNA blot analysis indicated that the transcripts of LLA-89 and LLA-142 were anther-specific and differentially detected in the anther wall and in the microspore of developing anthers. The LLA-89 gene could be exogenously induced by gibberellin while the LLA-142 gene could not. In situ hybridization with antisense riboprobes for the two genes in the anther revealed strong signals localized to the tapetal layer of the anther wall. The function of LLA-89 and LLA-142 genes was further discussed.
机译:从消减的cDNA文库中分离了两个阶段特异性基因,该文库由长百合的花药构建而成。使用聚合酶链反应(5'-和3'-RACE-PCR)对cDNA末端进行串联5'-和3'-快速扩增,以获得全长cDNA序列。 LLA-89 cDNA包含一个303 bp的开放阅读框,编码100个氨基酸的酸性多肽,计算分子量为10.2 kDa。 LLA-142 cDNA包含一个171 bp的开放阅读框,编码56个氨基酸的碱性多肽,计算分子量为5.7 kDa。 LLA-89 编码的蛋白在N端具有很强的疏水区,表明存在信号肽(在LLA-142蛋白中未发现)。序列比对揭示了由 LLA-142 编码的蛋白质是新颖的,而由 LLA-89 编码的蛋白质与报道的功能未知的LIM4蛋白质相同。总RNA印迹分析表明, LLA-89 和 LLA-142 的转录本是花药特异性的,并且在发育中的花药壁和花药小孢子中有差异。赤霉素可以外源诱导 LLA-89 基因,而 LLA-142 基因则不能。与花药中两个基因的反义核糖核酸进行的原位杂交揭示了强信号位于花药壁的绒毡层。进一步讨论了 LLA-89 和 LLA-142 基因的功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号