首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Gene sequence and expression of an analog of proliferating cell nuclear antigen (PCNA) in the alga Tetraselmis chui and detection of the encoded protein with anti-rat PCNA monoclonal antibody.
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Gene sequence and expression of an analog of proliferating cell nuclear antigen (PCNA) in the alga Tetraselmis chui and detection of the encoded protein with anti-rat PCNA monoclonal antibody.

机译:Tetraselmis chui藻中增殖细胞核抗原(PCNA)类似物的基因序列和表达并用抗大鼠PCNA单克隆抗体检测编码的蛋白。

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摘要

To identify a phytoplankton cell cycle marker detected by a monoclonal antibody against mammalian proliferating cell nuclear antigen (PCNA) (S. Lin, J. Chang, and E. J. Carpenter, J. Phycol. 30:449-456, 1994), a PCNA gene fragment was isolated by reverse transcription-PCR from the marine unicellular alga Tetraselmis chui Butcher (Prasinophyceae). The gene fragment was 616 bp in length and contained an open reading frame of 205 amino acids. The deduced amino acid sequence showed 80 and 88% similarity to human and rice PCNA, respectively. Southern hybridization indicated that the isolated gene fragment was part of the T. chui genome, with up to three copies in each haploid nucleus. Northern hybridization was used to detect a PCNA mRNA with a size of 1.2 kb from an exponentially growing algal culture. The T. chui gene fragment has been cloned into an expression vector, and a fusion protein was subsequently generated. Anti-rat PCNA simultaneously recognized the PCNA fusion protein and a single 33-kDa band in T.chui total protein extract. Our results indicate that T. chui PCNA is highly similar to its mammalian counterpart and that anti-rat PCNA is a good tool for detecting phytoplankton PCNA in general.
机译:鉴定通过针对哺乳动物增殖细胞核抗原(PCNA)的单克隆抗体检测到的浮游植物细胞周期标记(S. Lin,J. Chang和EJ Carpenter,J. Phycol。30:449-456,1994),一种PCNA基因通过逆转录-PCR从海洋单细胞藻Tetraselmis chui Butcher(Prasinophyceae)中分离片段。该基因片段长度为616 bp,包含一个205个氨基酸的开放阅读框。推导的氨基酸序列分别显示出与人和水稻PCNA的80%和88%的相似性。 Southern杂交表明,分离的基因片段是T. chui基因组的一部分,每个单倍体核中最多有3个拷贝。 Northern杂交用于从指数生长的藻类培养物中检测大小为1.2 kb的PCNA mRNA。 T. chui基因片段已被克隆到表达载体中,随后产生了融合蛋白。抗大鼠PCNA同时识别T.chui总蛋白提取物中的PCNA融合蛋白和一个33 kDa的条带。我们的结果表明,翠鸟PCNA与哺乳动物的PCNA非常相似,并且抗大鼠PCNA通常是检测浮游植物PCNA的良好工具。

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