Literature DB >> 7695743

Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes.

G Calabrese1, M Sallese, A Stornaiuolo, L Stuppia, G Palka, A De Blasi.   

Abstract

Two types of proteins play a major role in determining homologous desensitization of G-coupled receptors: beta-adrenergic receptor kinase (beta ARK), which phosphorylates the agonist-occupied receptor and its functional cofactor, beta-arrestin. Both beta ARK and beta-arrestin are members of multigene families. The family of G-protein-coupled receptor kinases includes rhodopsin kinase, beta ARK1, beta ARK2, IT11-A (GRK4), GRK5, and GRK6. The arrestin/beta-arrestin gene family includes arrestin (also known as S-antigen), beta-arrestin 1, and beta-arrestin 2. Here we report the chromosome mapping of the human genes for arrestin (SAG), beta-arrestin 2 (ARRB2), and beta ARK2 (ADRBK2) by fluorescence in situ hybridization (FISH). FISH results confirmed the assignment of the gene coding for arrestin (SAG) to chromosome 2 and allowed us to refine its localization to band q37. The gene coding for beta-arrestin 2 (ARRB2) was mapped to chromosome 17p13 and that coding for beta ARK2 (ADRBK2) to chromosome 22q11.

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Year:  1994        PMID: 7695743     DOI: 10.1006/geno.1994.1497

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  5 in total

1.  Chromosome mapping of the rat phospholipase C beta 1 gene.

Authors:  G Calabrese; R S Gilmour; L Stuppia; R Di Pietro; G Palka; L Cocco
Journal:  Mamm Genome       Date:  1995-08       Impact factor: 2.957

2.  Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p.

Authors:  A E Hughes; A J Lotery; G Silvestri
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

3.  A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.

Authors:  M Bayés; B Goldaracena; A Martínez-Mir; M I Iragui-Madoz; T Solans; P Chivelet; E Bussaglia; M A Ramos-Arroyo; M Baiget; L Vilageliu; S Balcells; R Gonzàlez-Duarte; D Grinberg
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

4.  Diagnosis of DiGeorge syndrome in nuclei released from archival autoptic heart specimens using fluorescence in situ hybridization.

Authors:  G Calabrese; R Mingarelli; P Francalanci; R Boldrini; G Palka; C Bosman; G Novelli; B Dallapiccola
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

5.  Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.

Authors:  A Pizzuti; G Novelli; A Mari; A Ratti; A Colosimo; F Amati; D Penso; F Sangiuolo; G Calabrese; G Palka; V Silani; M Gennarelli; R Mingarelli; G Scarlato; P Scambler; B Dallapiccola
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

  5 in total

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