Literature DB >> 17952705

Bulldog dwarfism in Dexter cattle is caused by mutations in ACAN.

Julie A L Cavanagh1, Imke Tammen, Peter A Windsor, John F Bateman, Ravi Savarirayan, Frank W Nicholas, Herman W Raadsma.   

Abstract

Bulldog dwarfism in Dexter cattle is one of the earliest single-locus disorders described in animals. Affected fetuses display extreme disproportionate dwarfism, reflecting abnormal cartilage development (chondrodysplasia). Typically, they die around the seventh month of gestation, precipitating a natural abortion. Heterozygotes show a milder form of dwarfism, most noticeably having shorter legs. Homozygosity mapping in candidate regions in a small Dexter pedigree suggested aggrecan (ACAN) as the most likely candidate gene. Mutation screening revealed a 4-bp insertion in exon 11 (2266_2267insGGCA) (called BD1 for diagnostic testing) and a second, rarer transition in exon 1 (-198C>T) (called BD2) that cosegregate with the disorder. In chondrocytes from cattle heterozygous for the insertion, mutant mRNA is subject to nonsense-mediated decay, showing only 8% of normal expression. Genotyping in Dexter families throughout the world shows a one-to-one correspondence between genotype and phenotype at this locus. The heterozygous and homozygous-affected Dexter cattle could prove invaluable as a model for human disorders caused by mutations in ACAN.

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Year:  2007        PMID: 17952705     DOI: 10.1007/s00335-007-9066-9

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  24 in total

Review 1.  Nonsense-mediated mRNA decay in health and disease.

Authors:  P A Frischmeyer; H C Dietz
Journal:  Hum Mol Genet       Date:  1999       Impact factor: 6.150

2.  The ins and outs of aggrecan.

Authors:  B M Vertel
Journal:  Trends Cell Biol       Date:  1995-12       Impact factor: 20.808

3.  The keratan sulfate-enriched region of bovine cartilage proteoglycan consists of a consecutively repeated hexapeptide motif.

Authors:  P Antonsson; D Heinegård; A Oldberg
Journal:  J Biol Chem       Date:  1989-09-25       Impact factor: 5.157

4.  Completion of the mouse aggrecan gene structure and identification of the defect in the cmd-Bc mouse as a near complete deletion of the murine aggrecan gene.

Authors:  R C Krueger; K Kurima; N B Schwartz
Journal:  Mamm Genome       Date:  1999-12       Impact factor: 2.957

5.  Species-specific alternative splicing of the epidermal growth factor-like domain 1 of cartilage aggrecan.

Authors:  C Fülöp; G Cs-Szabó; T T Glant
Journal:  Biochem J       Date:  1996-11-01       Impact factor: 3.857

6.  Chondrocytes from the cartilage proteoglycan-deficient mutant, nanomelia, synthesize greatly reduced levels of the proteoglycan core protein transcript.

Authors:  N S Stirpe; W S Argraves; P F Goetinck
Journal:  Dev Biol       Date:  1987-11       Impact factor: 3.582

Review 7.  The role of the extracellular matrix in skeletal development.

Authors:  S G Velleman
Journal:  Poult Sci       Date:  2000-07       Impact factor: 3.352

8.  The chondrodystrophy, nanomelia: biosynthesis and processing of the defective aggrecan precursor.

Authors:  B M Vertel; B L Grier; H Li; N B Schwartz
Journal:  Biochem J       Date:  1994-07-01       Impact factor: 3.857

9.  Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene.

Authors:  H Watanabe; K Kimata; S Line; D Strong; L Y Gao; C A Kozak; Y Yamada
Journal:  Nat Genet       Date:  1994-06       Impact factor: 38.330

10.  Disrupted expression of matrix genes in the growth plate of the mouse cartilage matrix deficiency (cmd) mutant.

Authors:  A W Wai; L J Ng; H Watanabe; Y Yamada; P P Tam; K S Cheah
Journal:  Dev Genet       Date:  1998
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  27 in total

Review 1.  The different roles of aggrecan interaction domains.

Authors:  Anders Aspberg
Journal:  J Histochem Cytochem       Date:  2012-09-26       Impact factor: 2.479

2.  A missense mutation in the aggrecan C-type lectin domain disrupts extracellular matrix interactions and causes dominant familial osteochondritis dissecans.

Authors:  Eva-Lena Stattin; Fredrik Wiklund; Karin Lindblom; Patrik Onnerfjord; Björn-Anders Jonsson; Yelverton Tegner; Takako Sasaki; André Struglics; Stefan Lohmander; Niklas Dahl; Dick Heinegård; Anders Aspberg
Journal:  Am J Hum Genet       Date:  2010-02-04       Impact factor: 11.025

3.  Structural variant-based pangenome construction has low sensitivity to variability of haplotype-resolved bovine assemblies.

Authors:  Alexander S Leonard; Danang Crysnanto; Zih-Hua Fang; Michael P Heaton; Brian L Vander Ley; Carolina Herrera; Heinrich Bollwein; Derek M Bickhart; Kristen L Kuhn; Timothy P L Smith; Benjamin D Rosen; Hubert Pausch
Journal:  Nat Commun       Date:  2022-05-31       Impact factor: 17.694

4.  Whole-genome sequencing reveals a potential causal mutation for dwarfism in the Miniature Shetland pony.

Authors:  Julia Metzger; Alana Christina Gast; Rahel Schrimpf; Janina Rau; Deborah Eikelberg; Andreas Beineke; Maren Hellige; Ottmar Distl
Journal:  Mamm Genome       Date:  2016-12-09       Impact factor: 2.957

5.  A nonsense mutation in cGMP-dependent type II protein kinase (PRKG2) causes dwarfism in American Angus cattle.

Authors:  James E Koltes; Bishnu P Mishra; Dinesh Kumar; Ranjit S Kataria; Liviu R Totir; Rohan L Fernando; Rowland Cobbold; David Steffen; Wouter Coppieters; Michel Georges; James M Reecy
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-03       Impact factor: 11.205

Review 6.  Aggrecan in Cardiovascular Development and Disease.

Authors:  Christopher D Koch; Chan Mi Lee; Suneel S Apte
Journal:  J Histochem Cytochem       Date:  2020-09-01       Impact factor: 2.479

7.  A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C-type lectin domain of aggrecan.

Authors:  Stuart W Tompson; Barry Merriman; Vincent A Funari; Maryline Fresquet; Ralph S Lachman; David L Rimoin; Stanley F Nelson; Michael D Briggs; Daniel H Cohn; Deborah Krakow
Journal:  Am J Hum Genet       Date:  2008-12-24       Impact factor: 11.025

8.  Description of the D4/D4 genotype in Miniature horses with dwarfism.

Authors:  Danilo G A Andrade; Roberta M Basso; Maria C R Castiglioni; Jeana P Silva; Vânia M V Machado; Renée Laufer-Amorim; Alexandre S Borges; José P Oliveira-Filho
Journal:  J Vet Diagn Invest       Date:  2020-01-06       Impact factor: 1.279

Review 9.  Genetic architecture of body size in mammals.

Authors:  Kathryn E Kemper; Peter M Visscher; Michael E Goddard
Journal:  Genome Biol       Date:  2012       Impact factor: 13.583

10.  Deletion in the EVC2 gene causes chondrodysplastic dwarfism in Tyrolean Grey cattle.

Authors:  Leonardo Murgiano; Vidhya Jagannathan; Cinzia Benazzi; Marilena Bolcato; Barbara Brunetti; Luisa Vera Muscatello; Keren Dittmer; Christian Piffer; Arcangelo Gentile; Cord Drögemüller
Journal:  PLoS One       Date:  2014-04-14       Impact factor: 3.240

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