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在莱茵衣藻中表达一个光捕获叶绿素 a/b 结合蛋白的基因:光和醋酸盐的影响。

Expression of a gene for a light-harvesting chlorophyll a/b-binding protein in Chlamydomonas reinhardtii: effect of light and acetate.

机构信息

Section of Biochemistry, Molecular, and Cell Biology, Cornell University, 14853, Ithaca, NY, USA.

出版信息

Plant Mol Biol. 1987 Nov;9(6):547-63. doi: 10.1007/BF00020532.

DOI:10.1007/BF00020532
PMID:24277192
Abstract

In Chlamydomonas reinhardtii, the chlorophyll a/b-binding proteins of photosystem II are encoded in the nucleus by a small family of genes. We have studied the expression of one gene, which we call cabII-1, in a green-in-the-dark strain, which can synthesize chlorophyll in the dark or light, and in a yellow-in-the-dark mutant strain, which is able to make chlorophyll only in the light. In light/dark synchronized cultures of both strains, cabII-1 mRNA abundance increases during the first 6 h of a 12-h light phase, remains high for several hours, then declines. A variety of illumination conditions have been used to analyze the cabII-1 mRNA increase: continuous or intermittent red, blue, or white light, with or without 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU), an inhibitor of photosystem II. Our results suggest that light induces increased cabII-1 transcript abundance in two ways: 1) by virtue of its role in the light reactions of photosynthesis and 2) by a blue lightstimulated mechanism which is independent of photosynthesis.We have also examined the role of acetate in regulating cabII-1 mRNA levels in the dark. In both green- and yellow-in-the-dark strains, 15 mM Na-acetate, added to synchronized cells in the dark, induces an increase in cabII-1 mRNA abundance with a temporal accumulation pattern very similar to that induced by continuous white light. We suggest that by providing an energy source, acetate stimulates cellular growth, cell cycle progression, and increased cabII-1 mRNA abundance. Interestingly, in cells exposed to light, acetate inhibits the light-induced increase in cabII-1 mRNA abundance by a mechanism which is not yet understood.

摘要

在莱茵衣藻中,光合系统 II 的叶绿素 a/b 结合蛋白由一小家族核基因编码。我们研究了一个基因的表达情况,该基因我们称之为 cabII-1,在一种能够在黑暗或光照下合成叶绿素的绿藻-黑暗突变体中,以及在一种只能在光照下合成叶绿素的黄藻-黑暗突变体中。在两种菌株的光/暗同步培养物中,cabII-1mRNA 的丰度在 12 小时光相的前 6 小时内增加,持续数小时后下降。我们使用了各种光照条件来分析 cabII-1mRNA 的增加:连续或间歇的红光、蓝光或白光,有或没有 3-(3,4-二氯苯基)-1,1-二甲基脲(DCMU),一种光合系统 II 的抑制剂。我们的结果表明,光以两种方式诱导 cabII-1 转录物丰度的增加:1)通过其在光合作用光反应中的作用,2)通过一种蓝光刺激机制,该机制独立于光合作用。我们还研究了乙酸盐在黑暗中调节 cabII-1mRNA 水平的作用。在绿藻和黄藻-黑暗突变体中,15mM 的 Na-乙酸盐在黑暗中添加到同步细胞中,会诱导 cabII-1mRNA 丰度增加,其时间积累模式与连续白光诱导的模式非常相似。我们认为,通过提供能量来源,乙酸盐刺激细胞生长、细胞周期进程和 cabII-1mRNA 丰度的增加。有趣的是,在暴露于光的细胞中,乙酸盐通过一种尚未了解的机制抑制光诱导的 cabII-1mRNA 丰度增加。

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