EXPRESSION OF PHOTOSYNTHESIS GENES IN THE CYANOBACTERIUM SYNECHOCYSTIS SP PCC-6803 - PSAA-PSAB AND PSBA TRANSCRIPTS ACCUMULATE IN DARK-GROWN CELLS

被引:52
作者
SMART, LB
MCINTOSH, L
机构
[1] MICHIGAN STATE UNIV, US DOE, PLANT RES LAB, E LANSING, MI 48824 USA
[2] MICHIGAN STATE UNIV, DEPT BIOCHEM, E LANSING, MI 48824 USA
[3] MICHIGAN STATE UNIV, US DOE, GENET PROGRAM, E LANSING, MI 48824 USA
关键词
GENE EXPRESSION; HETEROTROPHIC GROWTH; LEUCINE ZIPPER; PHOTOSYSTEM-I; PHOTOSYSTEM-II;
D O I
10.1007/BF00037136
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
We have cloned and sequenced the psaA and psaB genes from the unicellular cyanobacterium Synechocystis sp. PCC 6803. These genes are arranged in tandem, are co-transcribed, and are highly homologous to the psaA and psab genes previously characterized. RNA was isolated from light-grown cells, from cells put in total darkness with and without glucose, and from cells grown under light-activated heterotrophic growth (LAHG) conditions. Quantitation of hybridization to northern blots revealed only a slight decrease in the accumulation of the psaA-psaB transcript in cells grown in complete darkness with glucose and in LAHG cells, relative to light-grown cells. Accumulation of the psbA transcript steadily declines through dark incubation, with a steady-state level in LAHG cells 28% of that in light-grown cells. Transcripts from psbD, psaD, and rbcLS accumulate in cells grown in complete darkness and in LAHG cells to approximately the same levels as in light-grown cells. Photosynthesis gene transcripts in cells grown in the dark without glucose were detected, but were highly degraded. Our data prove that transcripts from photosynthesis genes do accumulate in dark-grown Synechocystis 6803, which may allow for synthesis and assembly of photosystem (PS) I and PS II in the dark.
引用
收藏
页码:959 / 971
页数:13
相关论文
共 50 条
[1]   LIGHT-ACTIVATED HETEROTROPHIC GROWTH OF THE CYANOBACTERIUM SYNECHOCYSTIS SP STRAIN PCC-6803 - A BLUE-LIGHT-REQUIRING PROCESS [J].
ANDERSON, SL ;
MCINTOSH, L .
JOURNAL OF BACTERIOLOGY, 1991, 173 (09) :2761-2767
[2]  
BENGIS C, 1977, J BIOL CHEM, V252, P4564
[3]   A COMPLEMENTATION ANALYSIS OF RESTRICTION AND MODIFICATION OF DNA IN ESCHERICHIA COLI [J].
BOYER, HW ;
ROULLAND.D .
JOURNAL OF MOLECULAR BIOLOGY, 1969, 41 (03) :459-&
[4]   DIFFERENT AND RAPID RESPONSES OF 4 CYANOBACTERIAL PSBA TRANSCRIPTS TO CHANGES IN LIGHT-INTENSITY [J].
BUSTOS, SA ;
SCHAEFER, MR ;
GOLDEN, SS .
JOURNAL OF BACTERIOLOGY, 1990, 172 (04) :1998-2004
[5]   MOLECULAR-CLONING AND NUCLEOTIDE-SEQUENCE OF THE PSAA AND PSAB GENES OF THE CYANOBACTERIUM SYNECHOCOCCUS SP PCC-7002 [J].
CANTRELL, A ;
BRYANT, DA .
PLANT MOLECULAR BIOLOGY, 1987, 9 (05) :453-468
[6]   ORGANIZATION OF THE RICE CHLOROPLAST PSAA-PSAB-RPS14 GENE AND THE PRESENCE OF SEQUENCE HETEROGENEITY IN THIS GENE-CLUSTER [J].
CHEN, SCG ;
CHENG, MC ;
CHEN, J ;
HWANG, LY .
PLANT SCIENCE, 1990, 68 (02) :213-221
[7]  
CHITNIS PR, 1989, J BIOL CHEM, V264, P18374
[8]  
CHITNIS PR, 1989, J BIOL CHEM, V264, P18381
[9]   MUTANT PHENOTYPES SUPPORT A TRANS-SPLICING MECHANISM FOR THE EXPRESSION OF THE TRIPARTITE PSAA GENE IN THE C-REINHARDTII CHLOROPLAST [J].
CHOQUET, Y ;
GOLDSCHMIDTCLERMONT, M ;
GIRARDBASCOU, J ;
KUCK, U ;
BENNOUN, P ;
ROCHAIX, JD .
CELL, 1988, 52 (06) :903-913
[10]  
CUSHMAN JC, 1987, PROGR PHOTOSYNTHESIS, P667