Literature DB >> 9704026

Human gap junction protein connexin31: molecular cloning and expression analysis.

K Wenzel1, D Manthey, K Willecke, K H Grzeschik, O Traub.   

Abstract

We have isolated and characterized a human genomic clone containing the complete coding region of connexin31 (Cx31). Similar to rodent Cx31, the coding region of human Cx31 is completely contained within the second exon and consists of 810 nucleotides. The deduced human Cx31 polypeptide consists of 270 amino acids with a predicted molecular mass of 30.818 kDa. Its sequence is most similar to mouse Cx31 (82.6% identical amino acids) and rat (83.0% identical amino acids), but shows considerably fewer potential sites of phosphorylation. After Northern blot hybridization, two Cx31 transcripts of 2.2 and 1.8 kb were detected in total RNA of the human keratinocyte cell line HaCaT and two transcripts of 2.2 and 1.9 kb in total RNA of E6/E7 transfected human keratinocytes (HEK cells). Using affinity-purified rabbit antibodies to mouse Cx31, immunofluorescence analysis demonstrated relatively weak expression of human Cx31 in HaCaT and HEK cells. The Cx31 gene exists as a single copy gene in the human genome and was mapped to the chromosomal region 1p34-p36 by analyzing human-mouse somatic cell hybrids.

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Year:  1998        PMID: 9704026     DOI: 10.1006/bbrc.1998.9070

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  3 in total

1.  Synthesis and assembly of connexins in vitro into homomeric and heteromeric functional gap junction hemichannels.

Authors:  S Ahmad; J A Diez; C H George; W H Evans
Journal:  Biochem J       Date:  1999-04-15       Impact factor: 3.857

2.  Gjb3 Gene Mutations in Non-Syndromic Hearing Loss of Bloch, Kurd, and Turkmen Ethnicities in Iran.

Authors:  Farnoush Aliazami; Dariush Farhud; Marjan Zarif-Yeganeh; Siamak Salehi; Azam Hosseinipour; Roxana Sasanfar; Maryam Eslami
Journal:  Iran J Public Health       Date:  2020-11       Impact factor: 1.429

3.  Comparison of the Mutation Spectrum of Common Deafness-Causing Genes in 509 Patients With Nonsyndromic Hearing Loss in 4 Different Areas of China by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry.

Authors:  Yi Wang; Wencheng Chen; Zhizhong Liu; Wen Xing; Haiyan Zhang
Journal:  J Int Adv Otol       Date:  2021-11       Impact factor: 1.017

  3 in total

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