Molecular cloning of cDNA for a rat heart gap junction protein

1987 ◽  
Vol 19 ◽  
pp. S42-S42
Author(s):  
E BEYER
1987 ◽  
Vol 105 (6) ◽  
pp. 2621-2629 ◽  
Author(s):  
E C Beyer ◽  
D L Paul ◽  
D A Goodenough

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.


1993 ◽  
Vol 268 (1) ◽  
pp. 706-712
Author(s):  
D.M. Rup ◽  
R.D. Veenstra ◽  
H.Z. Wang ◽  
P.R. Brink ◽  
E.C. Beyer

2001 ◽  
Vol 221 (2) ◽  
pp. 238-247 ◽  
Author(s):  
Nicola Cason ◽  
Thomas W. White ◽  
Shaohong Cheng ◽  
Daniel A. Goodenough ◽  
Gunnar Valdimarsson

1991 ◽  
Vol 68 (6) ◽  
pp. 1638-1651 ◽  
Author(s):  
M J van Kempen ◽  
C Fromaget ◽  
D Gros ◽  
A F Moorman ◽  
W H Lamers

1998 ◽  
Vol 248 (3) ◽  
pp. 910-915 ◽  
Author(s):  
Keirut Wenzel ◽  
Dieter Manthey ◽  
Klaus Willecke ◽  
Karl-Heinz Grzeschik ◽  
Otto Traub

1993 ◽  
Vol 91 (3) ◽  
pp. 997-1004 ◽  
Author(s):  
K E Reed ◽  
E M Westphale ◽  
D M Larson ◽  
H Z Wang ◽  
R D Veenstra ◽  
...  

1989 ◽  
Vol 108 (2) ◽  
pp. 595-605 ◽  
Author(s):  
E C Beyer ◽  
J Kistler ◽  
D L Paul ◽  
D A Goodenough

Rat heart and other organs contain mRNA coding for connexin43, a polypeptide homologous to a gap junction protein from liver (connexin32). To provide direct evidence that connexin43 is a cardiac gap junction protein, we raised rabbit antisera directed against synthetic oligopeptides corresponding to two unique regions of its sequence, amino acids 119-142 and 252-271. Both antisera stained the intercalated disc in myocardium by immunofluorescence but did not react with frozen sections of liver. Immunocytochemistry showed anti-connexin43 staining of the cytoplasmic surface of gap junctions in isolated rat heart membranes but no reactivity with isolated liver gap junctions. Both antisera reacted with a 43-kD polypeptide in isolated rat heart membranes but did not react with rat liver gap junctions by Western blot analysis. In contrast, an antiserum to the conserved, possibly extracellular, sequence of amino acids 164-189 in connexin32 reacted with both liver and heart gap junction proteins on Western blots. These findings support a topological model of connexins with unique cytoplasmic domains but conserved transmembrane and extracellular regions. The connexin43-specific antisera were used by Western blots and immunofluorescence to examine the distribution of connexin43. They demonstrated reactivity consistent with gap junctions between ovarian granulosa cells, smooth muscle cells in uterus and other tissues, fibroblasts in cornea and other tissues, lens and corneal epithelial cells, and renal tubular epithelial cells. Staining with the anti-connexin43 antisera was never observed to colocalize with antibodies to other gap junctional proteins (connexin32 or MP70) in the same junctional plaques. Because of limitations in the resolution of the immunofluorescence, however, we were not able to determine whether individual cells ever simultaneously express more than one connexin type.


1992 ◽  
Vol 127 (1) ◽  
pp. 69-76 ◽  
Author(s):  
Eric C Beyer ◽  
Karen E Reed ◽  
Eileen M Westphale ◽  
H Lee Kanter ◽  
David M Larson

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