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PMID: 11094154 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Trp12, a novel Trp related protein from kidney.

FEBS letters ·Vol. 485 ·No. 2-3 ·2000-11-24 ·Pages 127-34

Wissenbach U, Bödding M, Freichel M, Flockerzi V

Abstract

A novel member of the transient receptor potential (Trp) family of ion channels, Trp12, was identified. The Trp12 mRNA is abundantly expressed in mouse kidney and encodes a protein of 871 amino acid residues. Trp12 transfected cells reveal an elevated cytosolic Ca(2+) and respond with a further increase of cytosolic Ca(2+) to perfusion with hypoosmotic solutions. The human orthologue of murine Trp12 was localized on a genomic clone derived from human chromosome 12. It is composed of 15 translated exons. The intron placement within that primary structure does not correlate with the previously postulated splice sites in transcripts encoding the stretch-inhibitable channel which shares a high degree of amino acid sequence identity with Trp12 and the vanilloid receptor type 1.

MeSH Terms
Amino Acid Sequence Animals CHO Cells Calcium/metabolism Calcium Channels/chemistry,genetics,physiology Cell Line Chromosomes, Human, Pair 12 Cloning, Molecular Codon Cricetinae Cytosol/metabolism DNA/analysis Exons Gene Expression Humans Hypotonic Solutions/pharmacology Introns Kidney/chemistry Mice Molecular Sequence Data Polymerase Chain Reaction RNA Splicing RNA, Messenger/analysis Sequence Homology TRPC Cation Channels Transfection
Chemicals
Calcium Channels Codon Hypotonic Solutions RNA, Messenger TRPC Cation Channels transient receptor potential cation channel, subfamily C, member 1 DNA Calcium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wissenbach U
Institut für Pharmakologie und Toxikologie der Universität des Saarlandes, D-66421 Homburg, Germany. [email protected]
Bödding M
Freichel M
Flockerzi V
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
2000-11-24
Pages
127-34
Language
English
Region
England
NLM ID
0155157
Subset
IM
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