PLANT PHYSIOLOGY · 1988 · 71 citations · 18 references
Life SciencesDevelopmental BiologyPlant SciencesEmbryogenesisEmbryologyGene ExpressionAbscisic Acid BiologyEmbryo DevelopmentEmbryonic InductionProtein PhosphorylationProtein SynthesisAbscisic Acid In Embryo DevelopmentAbscisic Acid Signaling In SeedsAbscisic Acid-mediated Embryo DevelopmentCdna CloningDevelopmental Regulation By Abscisic AcidIsoelectric PointTranslational Control By Phosphorylation
We have earlier identified a set of proteins of 23 to 25 kilodaltons (kD), covering an isoelectric point (pI) range of 6.2 to 8.2, which accumulate gradually during normal embryogenesis of Zea mays and disappear in early germination. These polypeptides can be induced prematurely in immature embryos by abscisic acid (ABA) treatment. We report here that the more acidic protein forms are due to post-translational phosphorylation of at least two polypeptides of 23 kD, pI 8.2 and 25 kD, pI 8.0. A polyclonal antiserum was obtained which recognizes all forms of both the 23-kD and 25-kD polypeptides. Recovery of cDNA clones corresponding to these proteins was accomplished by hybridization with cDNA made from size-selected mRNA enriched for these sequences. Hybrid selection experiments demonstrate that clone MA12 specifically hybridizes with mRNAs encoding the 23-kD and 25-kD protein set which are recognized by the antiserum. By Northern hybridization analysis, the RNA encoded by clone MA12 is shown to accumulate in mature embryos and to be induced in young embryos upon ABA incubation.
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A simple and very efficient method for generating cDNA libraries
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High-efficiency cloning of full-length cDNA.
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A bacterial clone synthesizing proinsulin.
Lydia Villa‐Komaroff, Argiris Efstratiadis, S Broome et al. · Proceedings of the National Academy of Sciences · 1978 · 515 citations · Full text
Biochemistry and Physiology of Abscisic Acid
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