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性信息素诱导物对尖细角毛藻-条纹角毛藻-滨海角毛藻复合体中性信息素基因表达的调控

Regulation of expression of the genes for a sex pheromone by an inducer of the sex pheromone in the Closterium peracerosum-strigosum-littorale complex.

作者信息

Sekimoto H, Sone Y, Fujii T

机构信息

Institute of Biological Sciences, University of Tsukuba, Ibaraki, Japan.

出版信息

Planta. 1994;193(1):137-44. doi: 10.1007/BF00191617.

DOI:10.1007/BF00191617
PMID:7764622
Abstract

A sex pheromone, protoplast-release-inducing protein (PR-IP), of the Closterium peracerosum-strigosum-littorale complex is known to induce the release of protoplasts from mating-type minus (Mt-) cells during sexual reproduction and to have two subunit polypeptides of 19 and 42 kDa. Here, we describe the regulation mechanism for the release of the PR-IP. The sex pheromone was fractionated to yield subunits of 19 and 42 kDa, respectively, and each subunit was treated with V8 protease and with CNBr. By reference to the partial amino-acid sequences of the digested polypeptides, oligo nucleotides were synthesized and used as primers for the combined reverse transcription-polymerase chain reaction. Amplified fragments of DNA, of 130 bp in the case of the 19-kDa subunit and of 330 bp in the case of the 42-kDa subunit, were obtained, sequenced, and used as probes to identify the respective transcripts. From the results of Northern hybridization, the sizes of transcripts were estimated to be 1.2 kb for the 19-kDa subunit and 1.4 kb for the 42-kDa subunit. These transcripts appeared transiently only when mating-type plus (mt+) cells were treated with another sex pheromone (PR-IP Inducer) for more than 4 h in the light. By immunoblotting with anti-42-kDa-subunit antiserum, it was shown that PR-IP accumulated gradually in the medium but not in the mt+ cells after treatment with PR-IP inducer in the light.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

已知纤细角毛藻-绳纹角毛藻-滨海角毛藻复合体的一种性信息素——原生质体释放诱导蛋白(PR-IP),能在有性生殖过程中诱导交配型减(Mt-)细胞释放原生质体,且该蛋白有19 kDa和42 kDa的两个亚基多肽。在此,我们描述了PR-IP释放的调控机制。将该性信息素分级分离,分别得到19 kDa和42 kDa的亚基,每个亚基用V8蛋白酶和溴化氰处理。参照消化后多肽的部分氨基酸序列,合成寡核苷酸并用作逆转录-聚合酶链反应的引物。获得了19 kDa亚基130 bp和42 kDa亚基330 bp的DNA扩增片段,进行测序并用作探针以鉴定各自的转录本。通过Northern杂交结果估计,19 kDa亚基转录本大小为1.2 kb,42 kDa亚基转录本大小为1.4 kb。这些转录本仅在光照下用另一种性信息素(PR-IP诱导剂)处理交配型加(mt+)细胞4小时以上时短暂出现。用抗42 kDa亚基抗血清进行免疫印迹分析表明,光照下用PR-IP诱导剂处理后,PR-IP在培养基中逐渐积累,但不在mt+细胞中积累。(摘要截短于250字)

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