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J Biol Chem, Vol. 274, Issue 21, 14716-14723, May 21, 1999
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From the A new mouse connexin gene has been isolated that
codes for a connexin protein of 505 amino acid residues. Based on the
predicted molecular mass of 57.115 kDa, it has been designated
connexin-57. Similar to most other mouse connexin genes, the coding
region of connexin-57 is not interrupted by introns and exists in the mouse genome as a single-copy gene. Within the connexin family, this
new gene shows highest sequence identity to porcine connexin-60 in the
Institut für Genetik,
Universität Bonn, 53117 Bonn, Germany, the
§ Department of Neuroscience, Albert Einstein College of
Medicine, New York 10461, the ¶ Laboratory of Excitable
Structures, Kaunas Medical University, Kaunas, Lithuania, and the
Laboratory of Molecular Microbiology, NIAID, National Institutes
of Health, Bethesda, Maryland 20892
group of connexins. The connexin-57 gene was mapped to a position
on mouse chromosome 4, 30 centimorgans proximal to a cluster of
previously mapped connexin genes. Low levels of connexin-57 mRNA
were detected in skin, heart, kidney, testis, ovary, intestine, and in
the mouse embryo after 8 days post coitum, but expression was not
detected in brain, sciatic nerve or liver. In order to analyze gene
function, the connexin-57 coding region was expressed by transfection
in human HeLa cells, where it restored homotypic intercellular transfer
of microinjected neurobiotin. Heterotypic transfer was observed between
HeLa connexin-57 transfectants and HeLa cells, expressing murine
connexin-43, -37, or -30.3. Double whole-cell voltage clamp analyses
revealed that HeLa-connexin-57 transfectants expressed about 10 times
more channels than parental HeLa cells. Voltage gating by
transjunctional and transmembrane voltages as well as unitary
conductance (~27 picosiemens) were different from intrinsic connexin
channels in parental HeLa cells.
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