TIGRINA d, required for regulating the biosynthesis of tetrapyrroles in barley, is an ortholog of the FLU gene of Arabidopsis thaliana

被引:39
作者
Lee, KP
Kim, C
Lee, DW
Apel, K [1 ]
机构
[1] ETH, Swiss Fed Inst Technol, Inst Plant Sci Plant Genet, CH-8092 Zurich, Switzerland
[2] Dongguk Univ, Dept Life Sci, Kyongsangbuk 780714, South Korea
关键词
FLU; protochlorophyllide; feedback control; Tigrina mutant; Arabidopsis;
D O I
10.1016/S0014-5793(03)00983-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Regulation of tetrapyrrole biosynthesis in higher plants has been attributed to negative feedback control of steps prior to delta-aminolevulinic acid (ALA) formation. One of the first mutants with a defect in this control had been identified in barley. The tigrina (tig) d mutant accumulates 10-15-fold higher amounts of protochlorophyllide than wild type, when grown in the dark. The identity of the TIGRINA d protein and its mode of action are not known yet. Initially this protein had been proposed to act as a repressor of genes that encode enzymes involved in early steps of ALA formation, but subsequent attempts to confirm this experimentally failed. Here we demonstrate that the TIGRINA d gene of barley is an ortholog of the FLU gene of Arabidopsis thaliana. The FLU protein is a nuclear-encoded plastid protein that plays a key role in negative feedback control of chlorophyll biosynthesis in higher plants. Sequencing of the FLU gene of barley revealed a frame shift mutation in the FLU gene of the tig d mutant that results in the loss of two tetratricopeptide repeats that in the FLU protein of Arabidopsis are essential for its biological activity. This mutation cosegregates strictly with the tigrina phenotype within the F1 population of a heterozygous tig d mutant, thus providing additional support for the flu gene being responsible for the tigrina phenotype of barley. (C) 2003 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:119 / 124
页数:6
相关论文
共 31 条
[1]  
Alscher RG, 1997, PHYSIOL PLANTARUM, V100, P224, DOI 10.1034/j.1399-3054.1997.1000203.x
[2]  
ANDREW TL, 1990, BIOSYNTHESIS HEME CH, P163
[3]  
[Anonymous], BIOSYNTHESIS HEME CO
[4]   Enzymes of chlorophyll biosynthesis [J].
Beale, SI .
PHOTOSYNTHESIS RESEARCH, 1999, 60 (01) :43-73
[5]  
BOO JC, 2000, J PLANT PHYSL, V157, P405
[6]   A rapid DNA minipreparation method suitable for AFLP and other PCR applications [J].
Chen, DH ;
Ronald, PC .
PLANT MOLECULAR BIOLOGY REPORTER, 1999, 17 (01) :53-57
[7]   The structure of the tetratricopeptide repeats of protein phosphatase 5: implications for TPR-mediated protein-protein interactions [J].
Das, AK ;
Cohen, PTW ;
Barford, D .
EMBO JOURNAL, 1998, 17 (05) :1192-1199
[8]   INDUCTION OF PORPHYRIN SYNTHESIS IN ETIOLATED BEAN-LEAVES BY CHELATORS OF IRON [J].
DUGGAN, J ;
GASSMAN, M .
PLANT PHYSIOLOGY, 1974, 53 (02) :206-215
[9]   CONTROL OF DELTA-AMINOLEVULINIC-ACID AND CHLOROPHYLL ACCUMULATION IN GREENING MAIZE LEAVES UPON LIGHT-DARK TRANSITIONS [J].
FLUHR, R ;
HAREL, E ;
KLEIN, S ;
MELLER, E .
PLANT PHYSIOLOGY, 1975, 56 (04) :497-501
[10]  
Granik S., 1959, PLANT PHYSIOL, V34, pXVIII