Abstract
Identification of key regulatory kinases in the intestinal epithelium are useful to understand the molecular mechanisms that underlie proliferation and differentiation in cells found in this compartment. We used the polymerase chain reaction (PCR) to amplify the catalytic kinase domain of serine-threonine kinases by employing degenerate primers and then screened an intestinal crypt cDNA library to clone and sequence the open reading frame of a novel serine-threonine kinase. This was then further characterized by Northern blot analysis and RNA in situ hybridization. This kinase, designated intestinal cell kinase, harbors a dual phosphorylation site found in mitogen-activating protein (MAP) kinases that is important for kinase activity.
Copyright 2000 Wiley-Liss, Inc.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Animals
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Base Sequence
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Cell Line
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Cells, Cultured
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Chromosome Mapping*
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Colon
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Female
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Gene Library
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Humans
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Intestinal Mucosa / cytology
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Intestinal Mucosa / enzymology*
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Intestine, Small
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Mice
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Mice, Inbred C57BL
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Mitogen-Activated Protein Kinases / chemistry
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Mitogen-Activated Protein Kinases / metabolism*
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Molecular Sequence Data
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Muridae
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Organ Specificity
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Phosphorylation
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Polymerase Chain Reaction
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Protein Serine-Threonine Kinases / chemistry
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Protein Serine-Threonine Kinases / genetics*
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Protein Serine-Threonine Kinases / metabolism*
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Protein-Tyrosine Kinases
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RNA, Messenger / genetics
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Sequence Alignment
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Sequence Homology, Amino Acid
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Sequence Homology, Nucleic Acid
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src-Family Kinases / chemistry
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src-Family Kinases / genetics*
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src-Family Kinases / metabolism*
Substances
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RNA, Messenger
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Protein-Tyrosine Kinases
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Ptk6 protein, mouse
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src-Family Kinases
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Cilk1 protein, mouse
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Protein Serine-Threonine Kinases
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Mitogen-Activated Protein Kinases