Consequences of a Deletion in dspA on Transcript Accumulation in Synechocystis sp. Strain PCC6803

Author:

Tu Chao-Jung1,Shrager Jeffrey1,Burnap Robert L.2,Postier Bradley L.2,Grossman Arthur R.1

Affiliation:

1. Department of Plant Biology, The Carnegie Institution of Washington, Stanford, California 94305

2. Department of Microbiology and Molecular Genetics, Oklahoma State University, Stillwater, Oklahoma 74078

Abstract

ABSTRACT A sensor histidine kinase of Synechococcus sp. strain PCC7942, designated nblS , was previously identified and shown to be critical for the acclimation of cells to high-light and nutrient limitation conditions and to influence the expression of a number of light-responsive genes. The nblS orthologue in Synechocystis sp. strain PCC6803 is designated dspA (also called hik33 ). We have generated a dspA null mutant and analyzed global gene expression in both the mutant and wild-type strains under high- and low-light conditions. The mutant is aberrant for the expression of many genes encoding proteins critical for photosynthesis, phosphate and carbon acquisition, and the amelioration of stress conditions. Furthermore, transcripts from a number of genes normally detected only during exposure of wild-type cells to high-light conditions become partially constitutive in the low-light-grown dspA mutant. Other genes for which transcripts decline upon exposure of wild-type cells to high light are already lower in the mutant during growth in low light. These results suggest that DspA may influence gene expression in both a positive and a negative manner and that the dspA mutant behaves as if it were experiencing stress conditions (e.g., high-light exposure) even when maintained at near-optimal growth conditions for wild-type cells. This is discussed with respect to the importance of DspA for regulating the responses of the cell to environmental cues.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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