W. Kong et al., Isolation and characterization of the human gene encoding I-to: further diversity by alternative mRNA splicing, AM J P-HEAR, 44(6), 1998, pp. H1963-H1970
Citations number
44
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
The transient outward K+ current (I-to) in the heart is responsible for the
initial phase of repolarization and for setting the plateau voltage of the
ventricular action potential. Recently, Kv4.3 has emerged as the leading c
andidate alpha-subunit gene that underlies I-to in larger mammals such as d
ogs and humans. we have cloned the human Kv4.3 homolog and describe a carbo
xyl-terminal splice variant that inserts 19 amino acids with a consensus pr
otein kinase C (PKC) phosphorylation site into the protein after the last m
embrane-spanning segment. The coding region of Kv4.3 is comprised of at lea
st five exons and is located on chromosome 1p13.3. In the basal state the b
asic biophysical properties of bath of the splice variants are identical.