Mg chelatase in chlorophyll synthesis and retrograde signaling in Chlamydomonas reinhardtii: CHLI2 cannot substitute for CHLI1

被引:22
作者
Brzezowski, Pawel [1 ]
Sharifi, Marina N. [2 ,3 ,4 ]
Dent, Rachel M. [2 ,3 ,5 ]
Morhard, Marius K. [1 ]
Niyogi, Krishna K. [2 ,3 ]
Grimm, Bernhard [1 ]
机构
[1] Humboldt Univ, Inst Biol Plant Physiol, Philippstr 13, D-10115 Berlin, Germany
[2] Univ Calif Berkeley, Howard Hughes Med Inst, Dept Plant & Microbial Biol, Berkeley, CA 94720 USA
[3] Lawrence Berkeley Natl Lab, Phys Biosci Div, Berkeley, CA 94720 USA
[4] Univ Chicago, Comm Canc Biol, Chicago, IL 60637 USA
[5] Univ Calif Berkeley, Sch Publ Hlth, Berkeley, CA 94720 USA
关键词
Chlamydomonas; CHLI; chloroplast retrograde signaling; Mg chelatase; protoporphyrin IX; tetrapyrrole biosynthesis pathway; NUCLEAR GENE-EXPRESSION; MAGNESIUM CHELATASE; PROTOPORPHYRIN IX; H-SUBUNIT; XANTHOPHYLL CYCLE; LIGHT INDUCTION; ARABIDOPSIS; CHLOROPLAST; BIOSYNTHESIS; ACCUMULATION;
D O I
10.1093/jxb/erw004
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
CHLI1 is indispensable for MgCh function in C. reinhardtii, while CHLI2 is not involved in MgCh activity. Inactivation of MgCh due to CHLI1 deficiency results in altered nuclear gene expression.The oligomeric Mg chelatase (MgCh), consisting of the subunits CHLH, CHLI, and CHLD, is located at the central site of chlorophyll synthesis, but is also thought to have an additional function in regulatory feedback control of the tetrapyrrole biosynthesis pathway and in chloroplast retrograde signaling. In Arabidopsis thaliana and Chlamydomonas reinhardtii, two genes have been proposed to encode the CHLI subunit of MgCh. While the role of CHLI1 in A. thaliana MgCh has been substantially elucidated, different reports provide inconsistent results with regard to the function of CHLI2 in Mg chelation and retrograde signaling. In the present report, the possible functions of both isoforms were analyzed in C. reinhardtii. Knockout of the CHLI1 gene resulted in complete loss of MgCh activity, absence of chlorophyll, acute light sensitivity, and, as a consequence, down-regulation of tetrapyrrole biosynthesis and photosynthesis-associated nuclear genes. These observations indicate a phenotypical resemblance of chli1 to the chlh and chld C. reinhardtii mutants previously reported. The key role of CHLI1 for MgCh reaction in comparison with the second isoform was confirmed by the rescue of chli1 with genomic CHLI1. Because CHLI2 in C. reinhardtii shows lower expression than CHLI1, strains overexpressing CHLI2 were produced in the chli1 background. However, no complementation of the chli1 phenotype was observed. Silencing of CHLI2 in the wild-type background did not result in any changes in the accumulation of tetrapyrrole intermediates or of chlorophyll. The results suggest that, unlike in A. thaliana, changes in CHLI2 content observed in the present studies do not affect formation and activity of MgCh in C. reinhardtii.
引用
收藏
页码:3925 / 3938
页数:14
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