Literature DB >> 8663509

Molecular cloning and functional expression of mouse connexin-30,a gap junction gene highly expressed in adult brain and skin.

E Dahl1, D Manthey, Y Chen, H J Schwarz, Y S Chang, P A Lalley, B J Nicholson, K Willecke.   

Abstract

A new gap junction gene isolated from the mouse genome codes for a connexin protein of 261 amino acids. Because of its theoretical molecular mass of 30.366 kDa, it is named connexin-30. Within the connexin gene family, this protein is most closely related to connexin-26 (77% amino acid sequence identity). The coding region of mouse connexin-30 is uninterrupted by introns and is detected in the mouse genome as a single copy gene that is assigned to mouse chromosome 14 by analysis of mouse x hamster somatic cell hybrids. Abundant amounts of connexin-30 mRNA (two transcripts of 2.0 and 2.3 kilobase pairs) were found after 4 weeks of postnatal development in mouse brain and skin. Microinjection of connexin-30 cRNA into Xenopus oocytes induced formation of functional gap junction channels that gated somewhat asymmetrically in response to transjunctional voltage and at significantly lower voltage (Vo = +38 and -46 mV) than the closely homologous connexin-26 channels (Vo = 89 mV). Heterotypic pairings of connexin-30 with connexin-26 and connexin-32 produced channels with highly asymmetric and rectifying voltage gating, respectively. This suggests that the polarity of voltage gating and the cationic selectivity of connexin-30 are similar to those of its closest homologue, connexin-26.

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Year:  1996        PMID: 8663509     DOI: 10.1074/jbc.271.30.17903

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  37 in total

1.  Different ionic selectivities for connexins 26 and 32 produce rectifying gap junction channels.

Authors:  T M Suchyna; J M Nitsche; M Chilton; A L Harris; R D Veenstra; B J Nicholson
Journal:  Biophys J       Date:  1999-12       Impact factor: 4.033

2.  Zebrafish cx30.3: identification and characterization of a gap junction gene highly expressed in the skin.

Authors:  Liang Tao; Adam M DeRosa; Thomas W White; Gunnar Valdimarsson
Journal:  Dev Dyn       Date:  2010-10       Impact factor: 3.780

3.  A potent antagonist antibody targeting connexin hemichannels alleviates Clouston syndrome symptoms in mutant mice.

Authors:  Yuanyuan Kuang; Veronica Zorzi; Damiano Buratto; Gaia Ziraldo; Flavia Mazzarda; Chiara Peres; Chiara Nardin; Anna Maria Salvatore; Francesco Chiani; Ferdinando Scavizzi; Marcello Raspa; Min Qiang; Youjun Chu; Xiaojie Shi; Yu Li; Lili Liu; Yaru Shi; Francesco Zonta; Guang Yang; Richard A Lerner; Fabio Mammano
Journal:  EBioMedicine       Date:  2020-06-15       Impact factor: 8.143

4.  Subconductance states of Cx30 gap junction channels: data from transfected HeLa cells versus data from a mathematical model.

Authors:  Rolf Vogel; Virginijus Valiunas; Robert Weingart
Journal:  Biophys J       Date:  2006-06-16       Impact factor: 4.033

Review 5.  Gap junctions couple astrocytes and oligodendrocytes.

Authors:  Jennifer L Orthmann-Murphy; Charles K Abrams; Steven S Scherer
Journal:  J Mol Neurosci       Date:  2008-05       Impact factor: 3.444

Review 6.  Glial connexins and gap junctions in CNS inflammation and disease.

Authors:  Tammy Kielian
Journal:  J Neurochem       Date:  2008-04-10       Impact factor: 5.372

7.  Biophysical properties of mouse connexin30 gap junction channels studied in transfected human HeLa cells.

Authors:  V Valiunas; D Manthey; R Vogel; K Willecke; R Weingart
Journal:  J Physiol       Date:  1999-09-15       Impact factor: 5.182

8.  Molecular markers for cell types of the inner ear and candidate genes for hearing disorders.

Authors:  S Heller; C A Sheane; Z Javed; A J Hudspeth
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-15       Impact factor: 11.205

9.  A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients.

Authors:  Mohammad Hamid; Morteza Karimipoor; Morteza Hashemzadeh Chaleshtori; Mohammad Taghi Akbari
Journal:  J Genet       Date:  2009-12       Impact factor: 1.166

10.  Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations.

Authors:  Jennifer L Orthmann-Murphy; Ettore Salsano; Charles K Abrams; Alberto Bizzi; Graziella Uziel; Mona M Freidin; Eleonora Lamantea; Massimo Zeviani; Steven S Scherer; Davide Pareyson
Journal:  Brain       Date:  2008-12-04       Impact factor: 13.501

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