SEPARATE PHOTOSENSORY PATHWAYS COREGULATE BLUE-LIGHT/ULTRAVIOLET-A-ACTIVATED PSBD-PSBC TRANSCRIPTION AND LIGHT-INDUCED D2 AND CP43 DEGRADATION IN BARLEY (HORDEUM-VULGARE) CHLOROPLASTS

被引:113
作者
CHRISTOPHER, DA
MULLET, JE
机构
关键词
D O I
10.1104/pp.104.4.1119
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
We studied the effects of spectral quality and fluence on the expression of several chloroplast-encoded photosynthesis genes and on the stability of their protein products in barley (Hordeum vulgare). During light-dependent chloroplast maturation, mRNA levels for psbD-psbC and psbA were maintained at higher levels compared with mRNAs encoding proteins for other photosynthesis functions (atpB, rbcL). Maintenance of psbD-psbC mRNA levels was accounted for by differential activation of the psbD-psbC light-responsive promoter by high-irradiance blue light and, secondarily, ultraviolet A (UV-A) radiation. Promoter activation was fluence dependent and required continuous illumination for 2 h at threshold fluences of 1.3 (blue light), 7.5 (white light), or 10 (UV-A) mu mol m(-2) s(-1). From immunoblot analysis experiments, we showed that the psbD-psbC gene products D2 and CP43 undergo light-mediated turnover similar to light-labile D1. Other photosynthesis proteins such as the beta subunit of ATP synthase and the large subunit of ribulose-1,5-bisphosphate carboxylase were relatively stable. In the absence of protein synthesis, D2 degradation paralleled the degradation of D1 (relative half-lives, 9.5-10 h). CP43 decay was about half of D2 and D1 decay. In contrast with activation of the light-responsive promoter, the fluence-dependent degradation of D1, D2, and CP43 required 50- to 100-fold higher fluences of photosynthetically active white, red, blue, or UV-A irradiation. We interpret the different fluence and wavelength requirements to indicate that separate photosensory systems regulate activation of psbD-psbC transcription and turnover of D1, D2, and CP43. We propose that a blue light/UV-A photosensory pathway activates the psbD-psbC light-responsive promoter, differentially maintaining the capacity of mature chloroplasts to synthesize D2 and CP43, which are damaged and turned over in illuminated plants.
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页码:1119 / 1129
页数:11
相关论文
共 36 条
[1]   PHOTOREGULATION OF THE COMPOSITION, FUNCTION, AND STRUCTURE OF THYLAKOID MEMBRANES [J].
ANDERSON, JM .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1986, 37 :93-136
[2]   TOO MUCH OF A GOOD THING - LIGHT CAN BE BAD FOR PHOTOSYNTHESIS [J].
BARBER, J ;
ANDERSSON, B .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (02) :61-66
[3]   LIGHT-REGULATED EXPRESSION OF THE PSBD GENE FAMILY IN SYNECHOCOCCUS-SP STRAIN PCC-7942 - EVIDENCE FOR THE ROLE OF DUPLICATED PSBD GENES IN CYANOBACTERIA [J].
BUSTOS, SA ;
GOLDEN, SS .
MOLECULAR & GENERAL GENETICS, 1992, 232 (02) :221-230
[4]   A NOVEL LIGHT-REGULATED PROMOTER IS CONSERVED IN CEREAL AND DICOT CHLOROPLASTS [J].
CHRISTOPHER, DA ;
KIM, M ;
MULLET, JE .
PLANT CELL, 1992, 4 (07) :785-798
[5]   PHOTOPROTECTION AND OTHER RESPONSES OF PLANTS TO HIGH LIGHT STRESS [J].
DEMMIGADAMS, B ;
ADAMS, WW .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1992, 43 :599-626
[6]   ACTIVE TRANSLATION OF THE D-1 PROTEIN OF PHOTOSYSTEM-II IN SENESCING LEAVES [J].
DROILLARD, MJ ;
BATE, NJ ;
ROTHSTEIN, SJ ;
THOMPSON, JE .
PLANT PHYSIOLOGY, 1992, 99 (02) :589-594
[7]   PHOTOINACTIVATION OF CATALASE OCCURS UNDER BOTH HIGH-TEMPERATURE AND LOW-TEMPERATURE STRESS CONDITIONS AND ACCOMPANIES PHOTOINHIBITION OF PHOTOSYSTEM-II [J].
FEIERABEND, J ;
SCHAAN, C ;
HERTWIG, B .
PLANT PHYSIOLOGY, 1992, 100 (03) :1554-1561
[8]   DEVELOPMENTAL REGULATION OF 2 GENES ENCODING RIBULOSE-BISPHOSPHATE CARBOXYLASE SMALL SUBUNIT IN PEA AND TRANSGENIC PETUNIA PLANTS - PHYTOCHROME RESPONSE AND BLUE-LIGHT INDUCTION [J].
FLUHR, R ;
CHUA, NH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2358-2362
[9]   BLUE-LIGHT REGULATES THE ACCUMULATION OF 2 PSBD-PSBC TRANSCRIPTS IN BARLEY CHLOROPLASTS [J].
GAMBLE, PE ;
MULLET, JE .
EMBO JOURNAL, 1989, 8 (10) :2785-2794
[10]  
GAMBLE PE, 1989, J BIOL CHEM, V264, P7236