Connexin43: a protein from rat heart homologous to a gap junction protein from liver

Northern blot analysis of rat heart mRNA probed with a cDNA coding for the principal polypeptide of rat liver gap junctions demonstrated a 3.0- kb band. This band was observed only after hybridization and washing using low stringency conditions; high stringency conditions abolished the hybridization. A rat heart cDNA library was screened with the same cDNA probe under the permissive hybridization conditions, and a single positive clone identified and purified. The clone contained a 220-bp insert, which showed 55% homology to the original cDNA probe near the 5' end. The 220-bp cDNA was used to rescreen a heart cDNA library under high stringency conditions, and three additional cDNAs that together spanned 2,768 bp were isolated. This composite cDNA contained a single 1,146-bp open reading frame coding for a predicted polypeptide of 382 amino acids with a molecular mass of 43,036 D. Northern analysis of various rat tissues using this heart cDNA as probe showed hybridization to 3.0-kb bands in RNA isolated from heart, ovary, uterus, kidney, and lens epithelium. Comparisons of the predicted amino acid sequences for the two gap junction proteins isolated from heart and liver showed two regions of high homology (58 and 42%), and other regions of little or no homology. A model is presented which indicates that the conserved sequences correspond to transmembrane and extracellular regions of the junctional molecules, while the nonconserved sequences correspond to cytoplasmic regions. Since it has been shown previously that the original cDNA isolated from liver recognizes mRNAs in stomach, kidney, and brain, and it is shown here that the cDNA isolated from heart recognizes mRNAs in ovary, uterus, lens epithelium, and kidney, a nomenclature is proposed which avoids categorization by organ of origin. In this nomenclature, the homologous proteins in gap junctions would be called connexins, each distinguished by its predicted molecular mass in kilodaltons. The gap junction protein isolated from liver would then be called connexin32; from heart, connexin43.

[1]  H. Bode,et al.  Selective disruption of gap junctional communication interferes with a patterning process in hydra. , 1987, Science.

[2]  C. Green,et al.  Topological analysis of the major protein in isolated intact rat liver gap junctions and gap junction-derived single membrane structures. , 1987, The Journal of biological chemistry.

[3]  R. Werner,et al.  Expression of functional cell-cell channels from cloned rat liver gap junction complementary DNA. , 1987, Science.

[4]  N. Gilula,et al.  Functional assembly of gap junction conductance in lipid bilayers: Demonstration that the major 27 kd protein forms the junctional channel , 1987, Cell.

[5]  L. Hood,et al.  The cardiac gap junction protein (Mr 47,000) has a tissue-specific cytoplasmic domain of Mr 17,000 at its carboxy-terminus. , 1987, Biochemical and biophysical research communications.

[6]  R. Hynes,et al.  The structure of human thrombospondin, an adhesive glycoprotein with multiple calcium-binding sites and homologies with several different proteins , 1986, The Journal of cell biology.

[7]  N. Gilula,et al.  Cloning and characterization of human and rat liver cDNAs coding for a gap junction protein , 1986, The Journal of cell biology.

[8]  E. Hertzberg,et al.  Isolated liver gap junctions: gating of transjunctional currents is similar to that in intact pairs of rat hepatocytes. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[9]  D. Paul Molecular cloning of cDNA for rat liver gap junction protein , 1986, The Journal of cell biology.

[10]  D. Spray,et al.  Electrophysiological properties of gap junctions between dissociated pairs of rat hepatocytes , 1986, The Journal of cell biology.

[11]  D. Goodenough,et al.  Rat lens cultures: MIP expression and domains of intercellular coupling. , 1986, Investigative ophthalmology & visual science.

[12]  P. Greengard,et al.  cAMP increases junctional conductance and stimulates phosphorylation of the 27-kDa principal gap junction polypeptide. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[13]  A. Zervos,et al.  Preparation of a gap junction fraction from uteri of pregnant rats: the 28-kD polypeptides of uterus, liver, and heart gap junctions are homologous , 1985, The Journal of cell biology.

[14]  L. Hood,et al.  The Mr 28,000 gap junction proteins from rat heart and liver are different but related. , 1985, The Journal of biological chemistry.

[15]  C. Manjunath,et al.  Cell biology and protein composition of cardiac gap junctions. , 1985, The American journal of physiology.

[16]  C. Peracchia,et al.  Permeability and gating of lens gap junction channels incorporated into liposomes. , 1985, Current eye research.

[17]  E. Hertzberg,et al.  Reduction of gap junctional conductance by microinjection of antibodies against the 27-kDa liver gap junction polypeptide. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[18]  M. Olson,et al.  A new method for purifying lambda DNA from phage lysates. , 1985, DNA.

[19]  E. Hertzberg,et al.  A protein homologous to the 27,000 dalton liver gap junction protein is present in a wide variety of species and tissues , 1984, Cell.

[20]  J. Revel,et al.  The major intrinsic protein (MIP) of the bovine lens fiber membrane: Characterization and structure based on cDNA cloning , 1984, Cell.

[21]  G. Brewer,et al.  Role of gangliosides in adhesion and conductance changes in large spherical model membranes. , 1984, Biochimica et biophysica acta.

[22]  K. Willecke,et al.  Gap junctions in several tissues share antigenic determinants with liver gap junctions. , 1984, The EMBO journal.

[23]  N. Gilula,et al.  Antibodies to gap-junctional protein selectively disrupt junctional communication in the early amphibian embryo , 1984, Nature.

[24]  S. Henikoff Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. , 1984, Gene.

[25]  B. Hoffman,et al.  A simple and very efficient method for generating cDNA libraries. , 1983, Gene.

[26]  R. Weingart,et al.  Ungulate cardiac Purkinje fibres: the influence of intracellular pH on the electrical cell‐to‐cell coupling , 1982, The Journal of physiology.

[27]  R. Doolittle,et al.  A simple method for displaying the hydropathic character of a protein. , 1982, Journal of molecular biology.

[28]  E. Daniel,et al.  Changes of gap junctions in myometrium of guinea pig at parturition and abortion. , 1982, Canadian journal of physiology and pharmacology.

[29]  A. S. Menko,et al.  Rapid and reversible reduction of junctional permeability in cells infected with a temperature-sensitive mutant of avian sarcoma virus , 1981, The Journal of cell biology.

[30]  D. Goodenough,et al.  Five-hour half-life of mouse liver gap-junction protein , 1981, The Journal of cell biology.

[31]  W. Rutter,et al.  Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. , 1979, Biochemistry.

[32]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[33]  J. Piatigorsky,et al.  Rates of protein synthesis in explanted embryonic chick lens epithelia: differential stimulation of delta-crystallin synthesis. , 1975, Developmental biology.

[34]  David F. Albertini,et al.  THE APPEARANCE AND STRUCTURE OF INTERCELLULAR CONNECTIONS DURING THE ONTOGENY OF THE RABBIT OVARIAN FOLLICLE WITH PARTICULAR REFERENCE TO GAP JUNCTIONS , 1974, The Journal of cell biology.

[35]  B. Slatko,et al.  Sequencing in the fast lane: a rapid protocol for [α-35S] dATP dideoxy DNA sequencing , 1986 .

[36]  W. Loewenstein,et al.  Correction of cell–cell communication defect by introduction of a protein kinase into mutant cells , 1983, Nature.

[37]  J. Revel,et al.  The dynamic state of liver gap junctions. , 1981, Journal of supramolecular structure and cellular biochemistry.