Horticulture Department and Genetics Graduate Program, Clemson University;
Am J Bot. 2004 Feb;91(2):184-91. doi: 10.3732/ajb.91.2.184.
Using differential display of mRNA transcripts, we obtained a partial cDNA clone, RSC5-U, that is upregulated by exposure to high salinity. A longer cDNA of 812 nucleotides, designated HaABRC5, was then cloned by rapid amplification of cDNA ends. This full-length cDNA contains an open reading frame of 423 nucleotides encoding 141 amino acids, including a "bipartite nuclear targeting sequence." The deduced amino acid sequence had no similarity to known genes in the database. The expression of HaABRC5 was investigated in more detail using quantitative reverse transcriptase-polymerase chain reaction. HaABRC5 is upregulated by drought, high salinity, and exogenous application of abscisic acid (ABA). The promoter sequence of 229 nucleotides, upstream of HaABRC5, was cloned using rapid amplification of genomic ends. Three ABA-responsive elements were found within the HaABRC5 promoter region. Therefore, HaABRC5 is probably an ABA-responsive nuclear protein playing a role in plant stress response.
利用 mRNA 转录物的差异显示技术,我们获得了一个部分 cDNA 克隆,RSC5-U,其表达水平受到高盐胁迫的诱导而上调。通过快速扩增 cDNA 末端,进一步克隆得到了一个 812 个核苷酸的全长 cDNA,命名为 HaABRC5。该全长 cDNA 包含一个 423 个核苷酸的开放阅读框,编码 141 个氨基酸,包括一个“二分体核靶向序列”。该推导的氨基酸序列与数据库中的已知基因没有相似性。使用定量逆转录聚合酶链反应更详细地研究了 HaABRC5 的表达。HaABRC5 的表达受到干旱、高盐和外源脱落酸(ABA)的诱导上调。使用基因组末端快速扩增技术克隆了 HaABRC5 上游的 229 个核苷酸启动子序列。在 HaABRC5 启动子区域内发现了三个 ABA 反应元件。因此,HaABRC5 可能是一种 ABA 反应性核蛋白,在植物应激反应中发挥作用。