Literature DB >> 8825633

Molecular cloning of human G alpha q cDNA and chromosomal localization of the G alpha q gene (GNAQ) and a processed pseudogene.

Q Dong1, A Shenker, J Way, B R Haddad, K Lin, M R Hughes, O W McBride, A M Spiegel, J Battey.   

Abstract

G alpha q is the alpha subunit of one of the heterotrimeric GTP-binding proteins that mediates stimulation of phospholipase C beta. We report the isolation and characterization of cDNA clones from a frontal cortex cDNA library encoding human G alpha q. The encoded protein is 359 amino acids long and is identical in all but one amino acid residue to mouse G alpha q. Analysis of human genomic DNA reveals an intronless sequence with strong homology to human G alpha q cDNA. In comparison to G alpha q cDNA, this genomic DNA sequence includes several small deletions and insertions that alter the reading frame, multiple single base changes, and a premature termination codon in the open reading frame, hallmarks of a processed pseudogene. Probes derived from human G alpha q cDNA sequence map to both chromosomes 2 and 9 in high-stringency genomic blot analyses of DNA from a panel of human-rodent hybrid cell lines. PCR primers that selectively amplify the pseudogene sequence generate a product only when DNA containing human chromosome 2 is used as the template, indicating that the authentic G alpha q gene (GNAQ) is located on chromosome 9. Regional localization by FISH analysis places GNAQ at 9q21 and the pseudogene at 2q14.3-q21.

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Year:  1995        PMID: 8825633     DOI: 10.1006/geno.1995.1267

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


  5 in total

1.  Microarray profile of brain aging-related genes in the frontal cortex of SAMP8.

Authors:  Shao-Chun Chen; Gang Lu; Chu-Yan Chan; Yangchao Chen; Hua Wang; David Tai-Wai Yew; Zhong-Tang Feng; Hsiang-Fu Kung
Journal:  J Mol Neurosci       Date:  2009-10-17       Impact factor: 3.444

2.  The somatic GNAQ mutation c.548G>A (p.R183Q) is consistently found in Sturge-Weber syndrome.

Authors:  Mitsuko Nakashima; Masakazu Miyajima; Hidenori Sugano; Yasushi Iimura; Mitsuhiro Kato; Yoshinori Tsurusaki; Noriko Miyake; Hirotomo Saitsu; Hajime Arai; Naomichi Matsumoto
Journal:  J Hum Genet       Date:  2014-11-06       Impact factor: 3.172

3.  GNAq mutations are not identified in papillary thyroid carcinomas and hyperfunctioning thyroid nodules.

Authors:  Clarissa A Cassol; Miao Guo; Shereen Ezzat; Sylvia L Asa
Journal:  Endocr Pathol       Date:  2010-12       Impact factor: 3.943

Review 4.  Improved discrimination of melanotic schwannoma from melanocytic lesions by combined morphological and GNAQ mutational analysis.

Authors:  Heidi V N Küsters-Vandevelde; Ilse A C H van Engen-van Grunsven; Benno Küsters; Marcory R C F van Dijk; Patricia J T A Groenen; Pieter Wesseling; Willeke A M Blokx
Journal:  Acta Neuropathol       Date:  2010-09-24       Impact factor: 17.088

5.  Lack of GNAQ and GNA11 Germ-Line Mutations in Familial Melanoma Pedigrees with Uveal Melanoma or Blue Nevi.

Authors:  Jason E Hawkes; Jennifer Campbell; Daniel Garvin; Lisa Cannon-Albright; Pamela Cassidy; Sancy A Leachman
Journal:  Front Oncol       Date:  2013-06-28       Impact factor: 6.244

  5 in total

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