Author(s): Kalifa Y, Gilad A, Konrad Z, Zaccai M, Scolnik PA, , Kalifa Y, Gilad A, Konrad Z, Zaccai M, Scolnik PA, , Kalifa Y, Gilad A, Konrad Z, Zaccai M, Scolnik PA, , Kalifa Y, Gilad A, Konrad Z, Zaccai M, Scolnik PA,
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Abstract Tomato (Lycopersicon esculantum) ASR1 (abscisic acid stress ripening protein), a small plant-specific protein whose cellular mode of action defies deduction based on its sequence or homology analyses, is one of numerous plant gene products with unknown biological roles that become over-expressed under water- and salt-stress conditions. Steady-state cellular levels of tomato ASR1 mRNA and protein are transiently increased following exposure of plants to poly(ethylene glycol), NaCl or abscisic acid. Western blot and indirect immunofluorescence analysis with anti-ASR1 antibodies demonstrated that ASR1 is present both in the cytoplasmic and nuclear subcellular compartments; approx. one-third of the total ASR1 protein could be detected in the nucleus. Nuclear ASR1 is a chromatin-bound protein, and can be extracted with 1 M NaCl, but not with 0.5\% Triton X-100. ASR1, overexpressed in Escherichia coli and purified to homogeneity, possesses zinc-dependent DNA-binding activity. Competitive-binding experiments and SELEX (systematic evolution of ligands by exponential enrichment) analysis suggest that ASR1 binds at a preferred DNA sequence.
This article was published in Biochem J
and referenced in Rice Research: Open Access