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      The Arabidopsis Somatic Embryogenesis Receptor Kinase 1 Gene Is Expressed in Developing Ovules and Embryos and Enhances Embryogenic Competence in Culture

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          Abstract

          We report here the isolation of the Arabidopsis SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE 1 (AtSERK1) gene and we demonstrate its role during establishment of somatic embryogenesis in culture. The AtSERK1 gene is highly expressed during embryogenic cell formation in culture and during early embryogenesis. The AtSERK1 gene is first expressed in planta during megasporogenesis in the nucleus of developing ovules, in the functional megaspore, and in all cells of the embryo sac up to fertilization. After fertilization, AtSERK1 expression is seen in all cells of the developing embryo until the heart stage. After this stage, AtSERK1 expression is no longer detectable in the embryo or in any part of the developing seed. Low expression is detected in adult vascular tissue. Ectopic expression of the full-length AtSERK1 cDNA under the control of the cauliflower mosaic virus 35S promoter did not result in any altered plant phenotype. However, seedlings that overexpressed theAtSERK1 mRNA exhibited a 3- to 4-fold increase in efficiency for initiation of somatic embryogenesis. Thus, an increased AtSERK1 level is sufficient to confer embryogenic competence in culture.

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          Basic local alignment search tool.

          A new approach to rapid sequence comparison, basic local alignment search tool (BLAST), directly approximates alignments that optimize a measure of local similarity, the maximal segment pair (MSP) score. Recent mathematical results on the stochastic properties of MSP scores allow an analysis of the performance of this method as well as the statistical significance of alignments it generates. The basic algorithm is simple and robust; it can be implemented in a number of ways and applied in a variety of contexts including straightforward DNA and protein sequence database searches, motif searches, gene identification searches, and in the analysis of multiple regions of similarity in long DNA sequences. In addition to its flexibility and tractability to mathematical analysis, BLAST is an order of magnitude faster than existing sequence comparison tools of comparable sensitivity.
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            Molecular Cloning : A Laboratory Manual

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              A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures

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                Author and article information

                Journal
                Plant Physiology
                American Society of Plant Biologists (ASPB)
                1532-2548
                0032-0889
                November 01 2001
                November 01 2001
                November 01 2001
                November 01 2001
                November 01 2001
                November 01 2001
                : 127
                : 3
                : 803-816
                Affiliations
                [1 ]Laboratory of Molecular Biology, Wageningen University, 6703HA Wageningen, The Netherlands (V.H., M.V.H., E.D.L.S., K.B., S.C.d.V.);
                [2 ]Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724 (J.-P.V.-C., U.G.); and
                [3 ]Department of Plant Biology, University of Zurich, Zurich CH-8008, Switzerland (U.G.)
                Article
                10.1104/pp.010324
                129253
                11706164
                6bc3a0f7-3974-45eb-8b10-d3f82a008c9d
                © 2001

                https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model

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