Molecular cloning, expression, functional characterization, chromosomal localization, and gene structure of junctate, a novel integral calcium binding protein of sarco(endo)plasmic reticulum membrane
S. Treves et al., Molecular cloning, expression, functional characterization, chromosomal localization, and gene structure of junctate, a novel integral calcium binding protein of sarco(endo)plasmic reticulum membrane, J BIOL CHEM, 275(50), 2000, pp. 39555-39568
Screening a cDNA library from human skeletal muscle and cardiac muscle with
a cDNA probe derived from junctin led to the isolation of two groups of cD
NA clones, The first group displayed a deduced amino acid sequence that is
84% identical to that of dog heart junctin, whereas the second group had a
single open reading frame that encoded a polypeptide with a predicted mass
of 33 kDa, whose first 78 NH2-terminal residues are identical to junctin wh
ereas its COOH terminus domain is identical to aspartyl beta -hydroxylase,
a member of the alpha -ketoglutarate-dependent dioxygenase family. We named
the latter amino acid sequence junctate, Northern blot analysis indicates
that junctate is expressed in a variety of human tissues including heart, p
ancreas, brain, lung, liver, kidney, and skeletal muscle, Fluorescence in s
itu hybridization analysis revealed that the genetic loci of junctin and ju
nctate map to the same cytogenetic band oh human chromosome 8, Analysis of
intron/exon boundaries of the genomic BAC clones demonstrate that junctin,
junctate, and aspartyl beta -hydroxylase result from alternative splicing o
f the same gene.
The predicted lumenal portion of junctate is enriched in negatively charged
residues and is able to bind calcium. Scatchard analysis of equilibrium Ca
-45(2+) binding in the presence of a physiological concentration of KCl dem
onstrate that junctate binds 21.0 mol of Ca2+/mol protein with a k(D) of 21
7 +/- 20 muM (n = 5), Tagging recombinant junctate with green fluorescent p
rotein and expressing the chimeric polypeptide in COS-7-transfected cells i
ndicates that junctate is located in endoplasmic reticulum membranes and th
at its presence increases the peak amplitude and transient calcium released
by activation of surface membrane receptors coupled to InsP(3) receptor ac
tivation.
Our study shows that alternative splicing of the same gene generates the fo
llowing functionally distinct proteins: an enzyme (aspartyl beta -hydroxyla
se), a structural protein of SR (junctin), and a membrane-bound calcium bin
ding protein (junctate).