Literature DB >> 2297530

Localisation of the gene encoding the catalytic gamma subunit of phosphorylase kinase to human chromosome bands 7p12-q21.

T A Jones1, E F da Cruz e Silva, N K Spurr, D Sheer, P T Cohen.   

Abstract

Skeletal muscle phosphorylase kinase has the structure (alpha beta gamma delta)4 where the alpha and beta subunits are regulatory components, the gamma subunit possesses catalytic activity and the delta subunit is identical to the calcium binding protein calmodulin. A rabbit skeletal muscle cDNA for the gamma subunit has been used to map the human gene (PYKG1) to 7p12-q21, by analysis of somatic cell hybrids and in situ hybridisation. The data suggest that the skeletal muscle gamma subunit gene is located just above the centromere of chromosome 7, with further cross-hybridising sequences at 7q21 and 11p11-14. The liver gamma subunit is distinct and its mRNA does not cross-hybridize with the skeletal muscle gamma subunit cDNA. These results indicate that autosomal human phosphorylase kinase deficiencies affecting both liver and muscle are likely to be caused by a defect in the autosomally determined beta subunit, rather than the gamma subunit.

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Year:  1990        PMID: 2297530     DOI: 10.1016/0167-4781(90)90017-v

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  9 in total

1.  cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis.

Authors:  J J Davidson; T Ozçelik; C Hamacher; P J Willems; U Francke; M W Kilimann
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-15       Impact factor: 11.205

2.  Autosomal recessive phosphorylase kinase deficiency in liver, caused by mutations in the gene encoding the beta subunit (PHKB).

Authors:  I E van den Berg; E A van Beurden; J B de Klerk; O P van Diggelen; H E Malingré; M M Boer; R Berger
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

Review 3.  Genetic deficiencies of the glycogen phosphorylase system.

Authors:  J Hendrickx; P J Willems
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

4.  Neural regulation of the formation of skeletal muscle phosphorylase kinase holoenzyme in adult and developing rat muscle.

Authors:  D C Ng; R C Carlsen; D A Walsh
Journal:  Biochem J       Date:  1997-08-01       Impact factor: 3.857

Review 5.  The regulation of glycogenolysis in the brain.

Authors:  Owen W Nadeau; Joseph D Fontes; Gerald M Carlson
Journal:  J Biol Chem       Date:  2018-02-26       Impact factor: 5.157

6.  X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase alpha subunit.

Authors:  I E van den Berg; E A van Beurden; H E Malingré; H K van Amstel; B T Poll-The; J A Smeitink; W H Lamers; R Berger
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

7.  Human cDNA encoding the muscle isoform of the phosphorylase kinase gamma subunit (PHKG1).

Authors:  M Wehner; M W Kilimann
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

8.  In Silico characterization of phosphorylase kinase: evidence for an alternate intronic polyadenylation site in PHKG1.

Authors:  Joni S Winchester; Eric C Rouchka; Naomi S Rowland; Nancy A Rice
Journal:  Mol Genet Metab       Date:  2007-08-09       Impact factor: 4.797

9.  The gamma phosphorylase kinase gene, Phkg, maps to mouse chromosome 5 near Gus.

Authors:  A J Maichele; J S Chamberlain
Journal:  Mamm Genome       Date:  1994-01       Impact factor: 2.957

  9 in total

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