Analysis of the kinase-related protein gene found at human chromosome 3q21 in a multi-gene cluster: Organization, expression, alternative splicing, and polymorphic marker
We report the amino acid sequence, genomic organization, tissue expression, and alternative splice patterns for the human kinase related protein (KRP) gene, as well as the discovery of a new CA repeat sequence polymorphic marker in an upstream intron of the myosin light chain kinase (MLCK) gene. The...
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| Published in | Journal of cellular biochemistry Vol. 75; no. 3; pp. 481 - 491 |
|---|---|
| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
New York
John Wiley & Sons, Inc
01.12.1999
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0730-2312 1097-4644 |
| DOI | 10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5 |
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| Abstract | We report the amino acid sequence, genomic organization, tissue expression, and alternative splice patterns for the human kinase related protein (KRP) gene, as well as the discovery of a new CA repeat sequence polymorphic marker in an upstream intron of the myosin light chain kinase (MLCK) gene. The KRP/MLCK genetic locus is a prototype for a recently discovered paradigm in which an independently regulated gene for a non‐enzymic protein is embedded within a larger gene for a signal transduction enzyme, and both classes of proteins are involved in the regulation of the same cellular structure. The MLCK/KRP gene cluster has been found only in higher vertebrates and is localized to human chromosome 3q21. The determination of the human KRP amino acid sequence through cDNA sequence analysis and its comparison to the exon/intron organization of the human KRP gene revealed an alternative splice pattern at the start of KRP exon 2, resulting in the insertion of a single glutamic acid in the middle of the protein. Examination of tissue distribution using Northern blot analysis revealed that the human expression pattern is more similar to the well‐characterized chicken KRP gene expression pattern than to rodent or rabbit. Unexpected differences of the human gene from other species is the apparent expression of the human gene products in adult cardiac muscle, an observation that was pursued further by the production of a site‐directed antiserum and immunohistochemistry analysis. The results reported here provide insight into the conserved and variable features of this late evolving genetic paradigm, raise new questions about the molecular aspects of cardiac muscle regulation, and provide tools needed for future clinical studies. The comparative analysis of the MLCK/KRP locus, combined with the recent discovery of a similar genomic relationship among other signal transduction proteins, suggest a diverse distribution of this theme among signal transduction systems in higher vertebrate genomes and indicate the utility of comparative genomics in revealing late evolving genetic paradigms. J. Cell. Biochem. 75:481–491, 1999. © 1999 Wiley‐Liss, Inc. |
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| AbstractList | We report the amino acid sequence, genomic organization, tissue expression, and alternative splice patterns for the human kinase related protein (KRP) gene, as well as the discovery of a new CA repeat sequence polymorphic marker in an upstream intron of the myosin light chain kinase (MLCK) gene. The KRP/MLCK genetic locus is a prototype for a recently discovered paradigm in which an independently regulated gene for a non-enzymic protein is embedded within a larger gene for a signal transduction enzyme, and both classes of proteins are involved in the regulation of the same cellular structure. The MLCK/KRP gene cluster has been found only in higher vertebrates and is localized to human chromosome 3q21. The determination of the human KRP amino acid sequence through cDNA sequence analysis and its comparison to the exon/intron organization of the human KRP gene revealed an alternative splice pattern at the start of KRP exon 2, resulting in the insertion of a single glutamic acid in the middle of the protein. Examination of tissue distribution using Northern blot analysis revealed that the human expression pattern is more similar to the well-characterized chicken KRP gene expression pattern than to rodent or rabbit. Unexpected differences of the human gene from other species is the apparent expression of the human gene products in adult cardiac muscle, an observation that was pursued further by the production of a site-directed antiserum and immunohistochemistry analysis. The results reported here provide insight into the conserved and variable features of this late evolving genetic paradigm, raise new questions about the molecular aspects of cardiac muscle regulation, and provide tools needed for future clinical studies. The comparative analysis of the MLCK/KRP locus, combined with the recent discovery of a similar genomic relationship among other signal transduction proteins, suggest a diverse distribution of this theme among signal transduction systems in higher vertebrate genomes and indicate the utility of comparative genomics in revealing late evolving genetic paradigms.We report the amino acid sequence, genomic organization, tissue expression, and alternative splice patterns for the human kinase related protein (KRP) gene, as well as the discovery of a new CA repeat sequence polymorphic marker in an upstream intron of the myosin light chain kinase (MLCK) gene. The KRP/MLCK genetic locus is a prototype for a recently discovered paradigm in which an independently regulated gene for a non-enzymic protein is embedded within a larger gene for a signal transduction enzyme, and both classes of proteins are involved in the regulation of the same cellular structure. The MLCK/KRP gene cluster has been found only in higher vertebrates and is localized to human chromosome 3q21. The determination of the human KRP amino acid sequence through cDNA sequence analysis and its comparison to the exon/intron organization of the human KRP gene revealed an alternative splice pattern at the start of KRP exon 2, resulting in the insertion of a single glutamic acid in the middle of the protein. Examination of tissue distribution using Northern blot analysis revealed that the human expression pattern is more similar to the well-characterized chicken KRP gene expression pattern than to rodent or rabbit. Unexpected differences of the human gene from other species is the apparent expression of the human gene products in adult cardiac muscle, an observation that was pursued further by the production of a site-directed antiserum and immunohistochemistry analysis. The results reported here provide insight into the conserved and variable features of this late evolving genetic paradigm, raise new questions about the molecular aspects of cardiac muscle regulation, and provide tools needed for future clinical studies. The comparative analysis of the MLCK/KRP locus, combined with the recent discovery of a similar genomic relationship among other signal transduction proteins, suggest a diverse distribution of this theme among signal transduction systems in higher vertebrate genomes and indicate the utility of comparative genomics in revealing late evolving genetic paradigms. We report the amino acid sequence, genomic organization, tissue expression, and alternative splice patterns for the human kinase related protein (KRP) gene, as well as the discovery of a new CA repeat sequence polymorphic marker in an upstream intron of the myosin light chain kinase (MLCK) gene. The KRP/MLCK genetic locus is a prototype for a recently discovered paradigm in which an independently regulated gene for a non‐enzymic protein is embedded within a larger gene for a signal transduction enzyme, and both classes of proteins are involved in the regulation of the same cellular structure. The MLCK/KRP gene cluster has been found only in higher vertebrates and is localized to human chromosome 3q21. The determination of the human KRP amino acid sequence through cDNA sequence analysis and its comparison to the exon/intron organization of the human KRP gene revealed an alternative splice pattern at the start of KRP exon 2, resulting in the insertion of a single glutamic acid in the middle of the protein. Examination of tissue distribution using Northern blot analysis revealed that the human expression pattern is more similar to the well‐characterized chicken KRP gene expression pattern than to rodent or rabbit. Unexpected differences of the human gene from other species is the apparent expression of the human gene products in adult cardiac muscle, an observation that was pursued further by the production of a site‐directed antiserum and immunohistochemistry analysis. The results reported here provide insight into the conserved and variable features of this late evolving genetic paradigm, raise new questions about the molecular aspects of cardiac muscle regulation, and provide tools needed for future clinical studies. The comparative analysis of the MLCK/KRP locus, combined with the recent discovery of a similar genomic relationship among other signal transduction proteins, suggest a diverse distribution of this theme among signal transduction systems in higher vertebrate genomes and indicate the utility of comparative genomics in revealing late evolving genetic paradigms. J. Cell. Biochem. 75:481–491, 1999. © 1999 Wiley‐Liss, Inc. We report the amino acid sequence, genomic organization, tissue expression, and alternative splice patterns for the human kinase related protein (KRP) gene, as well as the discovery of a new CA repeat sequence polymorphic marker in an upstream intron of the myosin light chain kinase (MLCK) gene. The KRP/MLCK genetic locus is a prototype for a recently discovered paradigm in which an independently regulated gene for a non-enzymic protein is embedded within a larger gene for a signal transduction enzyme, and both classes of proteins are involved in the regulation of the same cellular structure. The MLCK/KRP gene cluster has been found only in higher vertebrates and is localized to human chromosome 3q21. The determination of the human KRP amino acid sequence through cDNA sequence analysis and its comparison to the exon/intron organization of the human KRP gene revealed an alternative splice pattern at the start of KRP exon 2, resulting in the insertion of a single glutamic acid in the middle of the protein. Examination of tissue distribution using Northern blot analysis revealed that the human expression pattern is more similar to the well-characterized chicken KRP gene expression pattern than to rodent or rabbit. Unexpected differences of the human gene from other species is the apparent expression of the human gene products in adult cardiac muscle, an observation that was pursued further by the production of a site-directed antiserum and immunohistochemistry analysis. The results reported here provide insight into the conserved and variable features of this late evolving genetic paradigm, raise new questions about the molecular aspects of cardiac muscle regulation, and provide tools needed for future clinical studies. The comparative analysis of the MLCK/KRP locus, combined with the recent discovery of a similar genomic relationship among other signal transduction proteins, suggest a diverse distribution of this theme among signal transduction systems in higher vertebrate genomes and indicate the utility of comparative genomics in revealing late evolving genetic paradigms. |
| Author | Watterson, D. Martin Weiss, Curtis Van Eldik, Linda J. Schavocky, James P. Chlenski, Alexandre Shirinsky, Vladimir P. Haiech, Jacques Guo, Ling |
| Author_xml | – sequence: 1 givenname: D. Martin surname: Watterson fullname: Watterson, D. Martin email: m-watterson@ nwu.edu organization: Department of Molecular Pharmacology and Biological Chemistry, Northwestern University, Chicago, Illinois – sequence: 2 givenname: James P. surname: Schavocky fullname: Schavocky, James P. organization: Department of Molecular Pharmacology and Biological Chemistry, Northwestern University, Chicago, Illinois – sequence: 3 givenname: Ling surname: Guo fullname: Guo, Ling organization: Department of Molecular Pharmacology and Biological Chemistry, Northwestern University, Chicago, Illinois – sequence: 4 givenname: Curtis surname: Weiss fullname: Weiss, Curtis organization: Department of Molecular Pharmacology and Biological Chemistry, Northwestern University, Chicago, Illinois – sequence: 5 givenname: Alexandre surname: Chlenski fullname: Chlenski, Alexandre organization: Department of Molecular Pharmacology and Biological Chemistry, Northwestern University, Chicago, Illinois – sequence: 6 givenname: Vladimir P. surname: Shirinsky fullname: Shirinsky, Vladimir P. organization: Laboratory of Cell Motility, Institute of Experimental Cardiology, Russian Cardiology Research Center, Moscow, Russia – sequence: 7 givenname: Linda J. surname: Van Eldik fullname: Van Eldik, Linda J. organization: Department of Cell and Molecular Biology, Northwestern University, Chicago, Illinois – sequence: 8 givenname: Jacques surname: Haiech fullname: Haiech, Jacques organization: Pharmacologie et Physico-Chimie des Interactions Cellulaires et Moléculaires, Faculté de Pharmacie, Université Louis Pasteur, Strasbourg, France |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/10536370$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1002/(SICI)1097-4644(19980901)70:3<402::AID-JCB13>3.0.CO;2-M 10.1152/ajpcell.1998.274.5.C1188 10.1016/B978-0-08-092636-0.50007-4 10.1023/A:1018676832164 10.1073/pnas.80.22.6775 10.1006/geno.1995.9965 10.1128/MCB.12.5.2359 10.1016/S0021-9258(18)98513-3 10.1016/0014-5793(95)01048-J 10.1038/380538a0 10.1093/nar/25.17.3389 10.1046/j.1365-2443.1996.720272.x 10.1016/S0021-9258(19)85458-3 |
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| References | Smith AF, Bigsby RM, Word RA, Herring PB. 1998. A 310-bp promoter mediates smooth muscle cell-specific expression of telokin. Am J Physiol 274(Cell Physiol 43):C1188-C1195. Van Eldik LJ, Fok K-F, Erickson BW, Watterson DM. 1983. Engineering of site-directed antisera against vertebrate calmodulin by using synthetic peptide immunogens containing an immunoreactive site. Proc Natl Acad Sci USA 80:6775-6779. Medline Birukov KG, Schavocky JP, Shirinsky VP, Chibalina MV, Van Eldik LJ, Watterson DM. 1998. The organization of the genetic locus for chicken myosin light chain kinase is complex: multiple proteins are encoded and exhibit differential expression and localization. J Cell Biochem 70:402-413. Medline Richardson A, Parsons JT. 1996. A mechanism for regulation of the adhesion-associated protein tyrosine kinase pp125FAK. Nature 380:538-540. Medline Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ. 1997. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25:3389-3402. Medline Tohtong R, Rodriguez D, Maughan D, Simcox A. 1997. Analysis of cDNAs encoding Drosophila melanogaster myosin light chain kinase. J Muscle Res Cell Motil 18:43-56. Medline Hunter T, Plowman GD. 1997. The protein kinases of budding yeast: six score and more. TIBS 22:18-22. Medline Watterson DM, Collinge M, Lukas TJ, Van Eldik LJ, Birukov KG, Stepanova OV, Shirinsky VS. 1995. Multiple gene products are produced from a novel protein kinase transcription region. FEBS Lett 373:217-220. Medline Collinge M, Matrisian PE, Zimmer WE, Shattuck RL, Lukas TJ, Van Eldik LJ, Watterson DM. 1992. Structure and expression of a calcium-binding protein gene contained within a calmodulin-regulated protein kinase gene. Mol Cell Biol 12:2359-2371. Medline Shirinsky VP, Vorotnikov AV, Birukov KG, Nanaev AK, Collinge M, Lukas TJ, Sellers JR, Watterson DM. 1993. A kinase related protein stabilizes unphosphorylated smooth muscle myosin minifilaments in the presence of ATP. J Biol Chem 268:16578-16583. Medline Potier MC, Chelot E, Pekarsky Y, Gardiner K, Rossier J, Turnell WG. 1995. The human myosin light chain kinase (MLCK) from hippocampus: cloning, sequencing, expression, and localization to 3qcen-q21. Genomics 29:562-570. Medline Kojima S, Mishima M, Mabuchi I, Hotta Y. 1996. A single Drosophila melanogaster myosin light chain kinase gene produces multiple isoforms whose activities are differently regulated. Genes Cells 1:855-871. Medline Tan JL, Spudich JA. 1991. Characterization and bacterial expression of the Dictyostelium myosin light chain kinase cDNA. J Biol Chem 266:16044-16049. Medline 1991; 266 1997; 22 1997; 25 1998 1997; 18 1996 1996; 380 1998; 70 1996; 1 1983; 80 1995; 29 1993; 268 1995; 373 1992; 12 Van Eldik (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB14) 1983; 80 Altschul (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB1) 1997; 25 Tan (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB12) 1991; 266 Hunter (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB4) 1997; 22 Smith (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB11) 1998; 274(Cell Physio Tohtong (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB13) 1997; 18 Reese (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB8) 1996 Collinge (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB3) 1992; 12 Birukov (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB2) 1998; 70 Potier (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB7) 1995; 29 Richardson (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB9) 1996; 380 Shirinsky (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB10) 1993; 268 Kojima (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB5) 1996; 1 Lukas (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB6) 1998 Watterson (10.1002/(SICI)1097-4644(19991201)75:3<481::AID-JCB12>3.0.CO;2-5-BIB15) 1995; 373 |
| References_xml | – reference: Tan JL, Spudich JA. 1991. Characterization and bacterial expression of the Dictyostelium myosin light chain kinase cDNA. J Biol Chem 266:16044-16049. Medline – reference: Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ. 1997. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25:3389-3402. Medline – reference: Potier MC, Chelot E, Pekarsky Y, Gardiner K, Rossier J, Turnell WG. 1995. The human myosin light chain kinase (MLCK) from hippocampus: cloning, sequencing, expression, and localization to 3qcen-q21. Genomics 29:562-570. Medline – reference: Collinge M, Matrisian PE, Zimmer WE, Shattuck RL, Lukas TJ, Van Eldik LJ, Watterson DM. 1992. Structure and expression of a calcium-binding protein gene contained within a calmodulin-regulated protein kinase gene. Mol Cell Biol 12:2359-2371. Medline – reference: Tohtong R, Rodriguez D, Maughan D, Simcox A. 1997. Analysis of cDNAs encoding Drosophila melanogaster myosin light chain kinase. J Muscle Res Cell Motil 18:43-56. Medline – reference: Watterson DM, Collinge M, Lukas TJ, Van Eldik LJ, Birukov KG, Stepanova OV, Shirinsky VS. 1995. Multiple gene products are produced from a novel protein kinase transcription region. FEBS Lett 373:217-220. Medline – reference: Smith AF, Bigsby RM, Word RA, Herring PB. 1998. A 310-bp promoter mediates smooth muscle cell-specific expression of telokin. Am J Physiol 274(Cell Physiol 43):C1188-C1195. – reference: Hunter T, Plowman GD. 1997. The protein kinases of budding yeast: six score and more. TIBS 22:18-22. Medline – reference: Kojima S, Mishima M, Mabuchi I, Hotta Y. 1996. A single Drosophila melanogaster myosin light chain kinase gene produces multiple isoforms whose activities are differently regulated. Genes Cells 1:855-871. Medline – reference: Van Eldik LJ, Fok K-F, Erickson BW, Watterson DM. 1983. 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| SubjectTerms | Adult Alleles Alternative Splicing Amino Acid Sequence Animals Base Sequence calcium Calcium-Binding Proteins - genetics calmodulin cardiac muscle Chromosomes, Human, Pair 3 - genetics Dinucleotide Repeats DNA Primers - genetics DNA, Complementary - genetics Exons Gene Expression genome Humans Introns Kinesin Molecular Sequence Data Multigene Family Muscle Proteins - genetics myosin Myosin-Light-Chain Kinase - genetics polymorphism Polymorphism, Genetic protein kinase Rabbits signal transduction smooth muscle |
| Title | Analysis of the kinase-related protein gene found at human chromosome 3q21 in a multi-gene cluster: Organization, expression, alternative splicing, and polymorphic marker |
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