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An early embryonic product of the gene shaggy encodes a serine/threonine protein kinase related to the CDC28/cdc2+ subfamily
The product(s) of the gene shaggy (sgg) is required for seemingly unrelated events during the development of Drosophila melanogaster. In embryos, maternal and zygotically derived sgg products are required initially to construct a normal syncytial blastoderm and later for normal segmentation. Further...
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Published in: | The EMBO journal 1990-09, Vol.9 (9), p.2877-2884 |
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description | The product(s) of the gene shaggy (sgg) is required for seemingly unrelated events during the development of Drosophila melanogaster. In embryos, maternal and zygotically derived sgg products are required initially to construct a normal syncytial blastoderm and later for normal segmentation. Furthermore, in mutant animals a process of intercellular communication that is required for the segregation of the neural and epidermal lineage during the formation of the central nervous system and the adult peripheral nervous system is disrupted. Here we describe a transcription unit of approximately 40 kb lying within the cloned chromosomal interval 3B1, and provide evidence that it encodes the sgg+ function. Of seven developmentally regulated transcripts that are partially generated by alternative splicing, two seem to be responsible for early sgg activity. Sequence analysis of corresponding cDNA(s) predicts a protein of 514 amino acids with a canonical catalytic domain found in serine/threonine specific protein kinases, linked to an unusual region rich in Gly, Ala and Ser. A search for homologies as well as a comparative study of the kinase catalytic domain with that of other proteins, revealed that the protein kinase domain of sgg is distantly related to the members of the CDC28/cdc2+ subfamily of protein kinases, all of which play cardinal roles in the regulation of the yeast and mammalian cell cycles. Ubiquitous expression of sgg transcripts was found during embryonic stages. A possible role of the sgg protein in a signal transduction pathway necessary for intercellular communication at different stages of development is discussed. |
doi_str_mv | 10.1002/j.1460-2075.1990.tb07477.x |
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In embryos, maternal and zygotically derived sgg products are required initially to construct a normal syncytial blastoderm and later for normal segmentation. Furthermore, in mutant animals a process of intercellular communication that is required for the segregation of the neural and epidermal lineage during the formation of the central nervous system and the adult peripheral nervous system is disrupted. Here we describe a transcription unit of approximately 40 kb lying within the cloned chromosomal interval 3B1, and provide evidence that it encodes the sgg+ function. Of seven developmentally regulated transcripts that are partially generated by alternative splicing, two seem to be responsible for early sgg activity. Sequence analysis of corresponding cDNA(s) predicts a protein of 514 amino acids with a canonical catalytic domain found in serine/threonine specific protein kinases, linked to an unusual region rich in Gly, Ala and Ser. A search for homologies as well as a comparative study of the kinase catalytic domain with that of other proteins, revealed that the protein kinase domain of sgg is distantly related to the members of the CDC28/cdc2+ subfamily of protein kinases, all of which play cardinal roles in the regulation of the yeast and mammalian cell cycles. Ubiquitous expression of sgg transcripts was found during embryonic stages. A possible role of the sgg protein in a signal transduction pathway necessary for intercellular communication at different stages of development is discussed.</description><identifier>ISSN: 0261-4189</identifier><identifier>EISSN: 1460-2075</identifier><identifier>DOI: 10.1002/j.1460-2075.1990.tb07477.x</identifier><identifier>PMID: 2118107</identifier><identifier>CODEN: EMJODG</identifier><language>eng</language><publisher>London: Nature Publishing Group</publisher><subject>Amino Acid Sequence ; Animals ; Base Sequence ; Biological and medical sciences ; CDC2 Protein Kinase ; Cyclin-Dependent Kinase Inhibitor Proteins ; Drosophila melanogaster - enzymology ; Drosophila melanogaster - genetics ; Drosophila melanogaster - growth & development ; Embryo, Nonmammalian - enzymology ; Fundamental and applied biological sciences. Psychology ; Fungal Proteins - genetics ; Gene Library ; Genes ; Genes. 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In embryos, maternal and zygotically derived sgg products are required initially to construct a normal syncytial blastoderm and later for normal segmentation. Furthermore, in mutant animals a process of intercellular communication that is required for the segregation of the neural and epidermal lineage during the formation of the central nervous system and the adult peripheral nervous system is disrupted. Here we describe a transcription unit of approximately 40 kb lying within the cloned chromosomal interval 3B1, and provide evidence that it encodes the sgg+ function. Of seven developmentally regulated transcripts that are partially generated by alternative splicing, two seem to be responsible for early sgg activity. Sequence analysis of corresponding cDNA(s) predicts a protein of 514 amino acids with a canonical catalytic domain found in serine/threonine specific protein kinases, linked to an unusual region rich in Gly, Ala and Ser. A search for homologies as well as a comparative study of the kinase catalytic domain with that of other proteins, revealed that the protein kinase domain of sgg is distantly related to the members of the CDC28/cdc2+ subfamily of protein kinases, all of which play cardinal roles in the regulation of the yeast and mammalian cell cycles. Ubiquitous expression of sgg transcripts was found during embryonic stages. A possible role of the sgg protein in a signal transduction pathway necessary for intercellular communication at different stages of development is discussed.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>CDC2 Protein Kinase</subject><subject>Cyclin-Dependent Kinase Inhibitor Proteins</subject><subject>Drosophila melanogaster - enzymology</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - growth & development</subject><subject>Embryo, Nonmammalian - enzymology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal Proteins - genetics</subject><subject>Gene Library</subject><subject>Genes</subject><subject>Genes. Genome</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>Phosphoproteins - genetics</subject><subject>Protein Kinases - genetics</subject><subject>Restriction Mapping</subject><subject>Saccharomyces cerevisiae Proteins</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Transcription, Genetic</subject><issn>0261-4189</issn><issn>1460-2075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNqVkc2O0zAURiMEGsrAIyBZSLBBSW0ntmMkFqUMfxrEBtaW49y0LondsROYSDw8yTQqsGRlS9_5rq91kuQZwRnBmK4PGSk4TikWLCNS4qyvsCiEyG7vJatzdD9ZYcpJWpBSPkwexXjAGLNSkIvkghJSEixWya-NQ6BDOyLoqjB6Zw06Bl8Ppke-Qf0e0A4coLjXu90EOeNriEijCME6WPf7AFNpIqZWD9ah79bpCChAq3uoUe_vhmzfbmm5NrWhL1EcqkZ3th0fJw8a3UZ4spyXybd3V1-3H9LrL-8_bjfXqWG4FCnRQteV4RUV1Jia45zw3ADTdPo2y5sC84LXtGpKI2vGZSk1cIJJRXTRQEXyy-T1ae5xqDqoDbg-6FYdg-10GJXXVv2bOLtXO_9DMUYxnvsvln7wNwPEXnU2Gmhb7cAPUQkpeU5xPoGvTqAJPsYAzfkNgtWsTh3U7EfNftSsTi3q1O1Ufvr3lufq4mrKny-5jka3TdDO2PjnBZlTJlk5cZsT99O2MP7HBurq85tPd_f8N2j3uQ4</recordid><startdate>199009</startdate><enddate>199009</enddate><creator>Bourouis, M.</creator><creator>Moore, P.</creator><creator>Ruel, L.</creator><creator>Grau, Y.</creator><creator>Heitzler, P.</creator><creator>Simpson, P.</creator><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>199009</creationdate><title>An early embryonic product of the gene shaggy encodes a serine/threonine protein kinase related to the CDC28/cdc2+ subfamily</title><author>Bourouis, M. ; Moore, P. ; Ruel, L. ; Grau, Y. ; Heitzler, P. ; Simpson, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5087-1a7adbc6b272ccd603163ce5a2b0753f40646d2bf8c9d56989ae6101b1a4feb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>CDC2 Protein Kinase</topic><topic>Cyclin-Dependent Kinase Inhibitor Proteins</topic><topic>Drosophila melanogaster - enzymology</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - growth & development</topic><topic>Embryo, Nonmammalian - enzymology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fungal Proteins - genetics</topic><topic>Gene Library</topic><topic>Genes</topic><topic>Genes. Genome</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>Phosphoproteins - genetics</topic><topic>Protein Kinases - genetics</topic><topic>Restriction Mapping</topic><topic>Saccharomyces cerevisiae Proteins</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bourouis, M.</creatorcontrib><creatorcontrib>Moore, P.</creatorcontrib><creatorcontrib>Ruel, L.</creatorcontrib><creatorcontrib>Grau, Y.</creatorcontrib><creatorcontrib>Heitzler, P.</creatorcontrib><creatorcontrib>Simpson, P.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The EMBO journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bourouis, M.</au><au>Moore, P.</au><au>Ruel, L.</au><au>Grau, Y.</au><au>Heitzler, P.</au><au>Simpson, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An early embryonic product of the gene shaggy encodes a serine/threonine protein kinase related to the CDC28/cdc2+ subfamily</atitle><jtitle>The EMBO journal</jtitle><addtitle>EMBO J</addtitle><date>1990-09</date><risdate>1990</risdate><volume>9</volume><issue>9</issue><spage>2877</spage><epage>2884</epage><pages>2877-2884</pages><issn>0261-4189</issn><eissn>1460-2075</eissn><coden>EMJODG</coden><abstract>The product(s) of the gene shaggy (sgg) is required for seemingly unrelated events during the development of Drosophila melanogaster. In embryos, maternal and zygotically derived sgg products are required initially to construct a normal syncytial blastoderm and later for normal segmentation. Furthermore, in mutant animals a process of intercellular communication that is required for the segregation of the neural and epidermal lineage during the formation of the central nervous system and the adult peripheral nervous system is disrupted. Here we describe a transcription unit of approximately 40 kb lying within the cloned chromosomal interval 3B1, and provide evidence that it encodes the sgg+ function. Of seven developmentally regulated transcripts that are partially generated by alternative splicing, two seem to be responsible for early sgg activity. Sequence analysis of corresponding cDNA(s) predicts a protein of 514 amino acids with a canonical catalytic domain found in serine/threonine specific protein kinases, linked to an unusual region rich in Gly, Ala and Ser. A search for homologies as well as a comparative study of the kinase catalytic domain with that of other proteins, revealed that the protein kinase domain of sgg is distantly related to the members of the CDC28/cdc2+ subfamily of protein kinases, all of which play cardinal roles in the regulation of the yeast and mammalian cell cycles. Ubiquitous expression of sgg transcripts was found during embryonic stages. A possible role of the sgg protein in a signal transduction pathway necessary for intercellular communication at different stages of development is discussed.</abstract><cop>London</cop><pub>Nature Publishing Group</pub><pmid>2118107</pmid><doi>10.1002/j.1460-2075.1990.tb07477.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Animals Base Sequence Biological and medical sciences CDC2 Protein Kinase Cyclin-Dependent Kinase Inhibitor Proteins Drosophila melanogaster - enzymology Drosophila melanogaster - genetics Drosophila melanogaster - growth & development Embryo, Nonmammalian - enzymology Fundamental and applied biological sciences. Psychology Fungal Proteins - genetics Gene Library Genes Genes. Genome Molecular and cellular biology Molecular genetics Molecular Sequence Data Phosphoproteins - genetics Protein Kinases - genetics Restriction Mapping Saccharomyces cerevisiae Proteins Sequence Homology, Nucleic Acid Transcription, Genetic |
title | An early embryonic product of the gene shaggy encodes a serine/threonine protein kinase related to the CDC28/cdc2+ subfamily |
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