Origin and evolution of the light-dependent protochlorophyllide oxidoreductase (LPOR) genes

被引:47
作者
Yang, J
Cheng, Q
机构
[1] Univ Cambridge, Dept Plant Sci, Cambridge CB2 3EA, England
[2] Peking Univ, Coll Life Sci, Beijing 100871, Peoples R China
关键词
protochlorophyllide reductase; cyanobacterial origin; endosymbiotic gene transfer;
D O I
10.1055/s-2004-821270
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Light-dependent NADPH-protochlorophyllide oxidoreductase (LPOR) is a nuclear-encoded chloroplast protein in green algae and higher plants which catalyzes the light-dependent reduction of protochlorophyllide to chlorophyllide. Light-dependent chlorophyll biosynthesis occurs in all oxygenic photosynthetic organisms. With the exception of angiosperms, this pathway coexists with a separate light-independent chlorophyll biosynthetic pathway, which is catalyzed by light-independent protochlorophyllide reductase (DPOR) in the dark. In contrast, the light-dependent function of chlorophyll biosynthesis is absent from anoxygenic photosynthetic bacteria. Consequently, the question is whether cyanobacteria are the ancestors of all organisms that conduct light-dependent chlorophyll biosynthesis. If so, how did photosynthetic eukaryotes acquire the homologous genes of LPOR in their nuclear genomes? The large number of complete genome sequences now available allow us to detect the evolutionary history of LPOR genes by conducting a genome-wide sequence comparison and phylogenetic analysis. Here, we show the results of a detailed phylogenetic analysis of LPOR and other functionally related enzymes in the short chain dehydrogenase/reductase (SDR) family. We propose that the LPOR gene originated in the cyanobacterial genome before the divergence of eukaryotic photosynthetic organisms. We postulated that the photosynthetic eukaryotes obtained their LPOR homologues through endosymbiotic gene transfer.
引用
收藏
页码:537 / 544
页数:8
相关论文
共 48 条
[1]   IDENTIFICATION OF NADPH-PROTOCHLOROPHYLLIDE OXIDOREDUCTASE-A AND OXIDOREDUCTASE-B - A BRANCHED PATHWAY FOR LIGHT-DEPENDENT CHLOROPHYLL BIOSYNTHESIS IN ARABIDOPSIS-THALIANA [J].
ARMSTRONG, GA ;
RUNGE, S ;
FRICK, G ;
SPERLING, U ;
APEL, K .
PLANT PHYSIOLOGY, 1995, 108 (04) :1505-1517
[2]   PURIFICATION OF THE ENZYME NADPH - PROTOCHLOROPHYLLIDE OXIDOREDUCTASE [J].
BEER, NS ;
GRIFFITHS, WT .
BIOCHEMICAL JOURNAL, 1981, 195 (01) :83-92
[3]   Nitrogen fixation and photosynthetic oxygen evolution in cyanobacteria [J].
Berman-Frank, I ;
Lundgren, P ;
Falkowski, P .
RESEARCH IN MICROBIOLOGY, 2003, 154 (03) :157-164
[4]   Ancient horizontal gene transfer [J].
Brown, JR .
NATURE REVIEWS GENETICS, 2003, 4 (02) :121-132
[5]   ROOT OF THE UNIVERSAL TREE OF LIFE BASED ON ANCIENT AMINOACYL-TRANSFER-RNA SYNTHETASE GENE DUPLICATIONS [J].
BROWN, JR ;
DOOLITTLE, WF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :2441-2445
[6]   EARLY EVOLUTION OF PHOTOSYNTHESIS - CLUES FROM NITROGENASE AND CHLOROPHYLL IRON PROTEINS [J].
BURKE, DH ;
HEARST, JE ;
SIDOW, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (15) :7134-7138
[7]  
CHENG Q, 1998, THESIS U E ANGLIA NO
[8]   The role of protein surface charge in catalytic activity and chloroplast membrane association of the pea NADPH: protochlorophyllide oxidoreductase (POR) as revealed by alanine scanning mutagenesis [J].
Dahlin, C ;
Aronsson, H ;
Wilks, HM ;
Lebedev, N ;
Sundqvist, C ;
Timko, MP .
PLANT MOLECULAR BIOLOGY, 1999, 39 (02) :309-323
[9]  
FORREITER C, 1993, PLANTA, V190, P536, DOI 10.1007/BF00224793
[10]   Cloning of the gene encoding a protochlorophyllide reductase:: the physiological significance of the co-existence of light-dependent and -independent protochlorophyllide reduction systems in the Cyanobacterium Plectonema boryanum [J].
Fujita, Y ;
Takagi, H ;
Hase, T .
PLANT AND CELL PHYSIOLOGY, 1998, 39 (02) :177-185