Reference : A nonsense mutation in cGMP-dependent type II protein kinase (PRKG2) causes dwarfism ...
Scientific journals : Article
Life sciences : Genetics & genetic processes
http://hdl.handle.net/2268/101965
A nonsense mutation in cGMP-dependent type II protein kinase (PRKG2) causes dwarfism in American Angus cattle.
English
Koltes, James E [> > > >]
Mishra, Bishnu P [> > > >]
Kumar, Dinesh [> > > >]
Kataria, Ranjit S [> > > >]
Totir, Liviu R [> > > >]
Fernando, Rohan L [> > > >]
Cobbold, Rowland [> > > >]
Steffen, David [> > > >]
Coppieters, Wouter mailto [Université de Liège - ULg > Département de productions animales > Département de productions animales]
Georges, Michel mailto [> > > >]
Reecy, James M [ > > ]
2009
Proceedings of the National Academy of Sciences of the United States of America
National Academy of Sciences
106
46
19250-5
Yes (verified by ORBi)
International
0027-8424
1091-6490
Washington
DC
[en] Amino Acid Sequence ; Animals ; Cattle ; Cells, Cultured ; Codon, Nonsense ; Collagen Type II/genetics ; Collagen Type X/genetics ; Cyclic GMP-Dependent Protein Kinases/genetics ; Dwarfism/genetics/veterinary ; Exons/genetics ; Gene Expression Regulation ; Growth Plate/metabolism ; Molecular Sequence Data ; RNA Stability/genetics ; RNA, Messenger/metabolism
[en] Historically, dwarfism was the major genetic defect in U.S. beef cattle. Aggressive culling and sire testing were used to minimize its prevalence; however, neither of these practices can eliminate a recessive genetic defect. We assembled a 4-generation pedigree to identify the mutation underlying dwarfism in American Angus cattle. An adaptation of the Elston-Steward algorithm was used to overcome small pedigree size and missing genotypes. The dwarfism locus was fine-mapped to BTA6 between markers AFR227 and BM4311. Four candidate genes were sequenced, revealing a nonsense mutation in exon 15 of cGMP-dependant type II protein kinase (PRKG2). This C/T transition introduced a stop codon (R678X) that truncated 85 C-terminal amino acids, including a large portion of the kinase domain. Of the 75 mutations discovered in this region, only this mutation was 100% concordant with the recessive pattern of inheritance in affected and carrier individuals (log of odds score = 6.63). Previous research has shown that PRKG2 regulates SRY (sex-determining region Y) box 9 (SOX9)-mediated transcription of collagen 2 (COL2). We evaluated the ability of wild-type (WT) or R678X PRKG2 to regulate COL2 expression in cell culture. Real-time PCR results confirmed that COL2 is overexpressed in cells that overexpressed R678X PRKG2 as compared with WT PRKG2. Furthermore, COL2 and COL10 mRNA expression was increased in dwarf cattle compared with unaffected cattle. These experiments indicate that the R678X mutation is functional, resulting in a loss of PRKG2 regulation of COL2 and COL10 mRNA expression. Therefore, we present PRKG2 R678X as a causative mutation for dwarfism cattle.
Researchers ; Professionals
http://hdl.handle.net/2268/101965
10.1073/pnas.0904513106

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