Literature DB >> 16416092

Fine-mapping and candidate gene analysis of bovine spinal muscular atrophy.

Stefan Krebs1, Ivica Medugorac, Ingolf Russ, Pete Ossent, Ulrich Bleul, Wolfgang Schmahl, Martin Förster.   

Abstract

Bovine spinal muscular atrophy (SMA), an autosomal recessive neurodegenerative disease, has been mapped at moderate resolution to the distal part of Chromosome 24. In this article we confirm this location and fine-map the SMA locus to an interval of approximately 0.8 cM at the very distal end of BTA24. Despite remarkable similarity to human SMA, the causative gene SMN can be excluded in bovine SMA. However, the interval where the disease now has been mapped contains BCL2, like SMN an antiapoptotic factor, and shown to bind to SMN. Moreover, knockout mice lacking the BCL2 gene show rapid motor neuron degeneration with early postnatal onset, as observed in bovine SMA. A comparative cattle/human map of the distal end of BTA24, based on the emerging bovine genome sequencing data, shows conserved synteny to HSA18 with hints of a segmental duplication and pericentric inversion just after the last available bovine marker DIK4971. This synteny lets us conclude that SMA is in immediate vicinity of the telomere. Candidate gene analysis of BCL2, however, excludes most of this gene, except its promoter region, and draws attention to the neighboring gene VPS4B, part of the endosomal protein-sorting machinery ESCRT-III which is involved in several neurodegenerative diseases.

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Year:  2006        PMID: 16416092     DOI: 10.1007/s00335-005-0102-3

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   3.224


  32 in total

1.  RNaseCut: a MALDI mass spectrometry-based method for SNP discovery.

Authors:  Stefan Krebs; Ivica Medugorac; Doris Seichter; Martin Förster
Journal:  Nucleic Acids Res       Date:  2003-04-01       Impact factor: 16.971

2.  Reduced numbers and intense anti-ubiquitin immunostaining of bovine motor neurons affected with spinal muscular atrophy.

Authors:  T Hiraga; H W Leipold; W C Cash; D L Troyer
Journal:  J Neurol Sci       Date:  1993-08       Impact factor: 3.181

Review 3.  Segmental duplications and the evolution of the primate genome.

Authors:  Rhea Vallente Samonte; Evan E Eichler
Journal:  Nat Rev Genet       Date:  2002-01       Impact factor: 53.242

4.  Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia.

Authors:  Gaia Skibinski; Nicholas J Parkinson; Jeremy M Brown; Lisa Chakrabarti; Sarah L Lloyd; Holger Hummerich; Jørgen E Nielsen; John R Hodges; Maria Grazia Spillantini; Tove Thusgaard; Sebastian Brandner; Arne Brun; Martin N Rossor; Anders Gade; Peter Johannsen; Sven Asger Sørensen; Susanne Gydesen; Elizabeth M C Fisher; John Collinge
Journal:  Nat Genet       Date:  2005-07-24       Impact factor: 38.330

5.  Faster sequential genetic linkage computations.

Authors:  R W Cottingham; R M Idury; A A Schäffer
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

6.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

7.  Inactivation of bcl-2 results in progressive degeneration of motoneurons, sympathetic and sensory neurons during early postnatal development.

Authors:  T M Michaelidis; M Sendtner; J D Cooper; M S Airaksinen; B Holtmann; M Meyer; H Thoenen
Journal:  Neuron       Date:  1996-07       Impact factor: 17.173

8.  Construction of multilocus genetic linkage maps in humans.

Authors:  E S Lander; P Green
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

9.  Amyotrophic lateral sclerosis-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria.

Authors:  Piera Pasinelli; Mary Elizabeth Belford; Niall Lennon; Brian J Bacskai; Bradley T Hyman; Davide Trotti; Robert H Brown
Journal:  Neuron       Date:  2004-07-08       Impact factor: 17.173

10.  A comprehensive genetic map of the cattle genome based on 3802 microsatellites.

Authors:  Naoya Ihara; Akiko Takasuga; Kazunori Mizoshita; Haruko Takeda; Mayumi Sugimoto; Yasushi Mizoguchi; Takashi Hirano; Tomohito Itoh; Toshio Watanabe; Kent M Reed; Warren M Snelling; Steven M Kappes; Craig W Beattie; Gary L Bennett; Yoshikazu Sugimoto
Journal:  Genome Res       Date:  2004-10       Impact factor: 9.043

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  3 in total

1.  A missense mutation in the 3-ketodihydrosphingosine reductase FVT1 as candidate causal mutation for bovine spinal muscular atrophy.

Authors:  Stefan Krebs; Ivica Medugorac; Susanne Röther; Katja Strässer; Martin Förster
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-09       Impact factor: 11.205

2.  Spinal Muscular Atrophy in Blonde D'Aquitaine Calves Is Not Associated With FVT1 Gene Mutation.

Authors:  Giulia Cagnotti; Carlo Cantile; Stefania Chessa; Paola Sacchi; Antonio D'Angelo; Claudio Bellino
Journal:  Front Vet Sci       Date:  2020-06-23

3.  An Integrative Transcriptomic Analysis for Identifying Novel Target Genes Corresponding to Severity Spectrum in Spinal Muscular Atrophy.

Authors:  Chung-Wei Yang; Chien-Lin Chen; Wei-Chun Chou; Ho-Chen Lin; Yuh-Jyh Jong; Li-Kai Tsai; Chun-Yu Chuang
Journal:  PLoS One       Date:  2016-06-22       Impact factor: 3.240

  3 in total

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