Deep Intronic Mutation and Pseudo Exon Activation as a Novel Muscular Hypertrophy Modifier in Cattle

被引:13
|
作者
Bouyer, Claire [1 ]
Forestier, Lionel [1 ]
Renand, Gilles [2 ]
Oulmouden, Ahmad [1 ]
机构
[1] Univ Limoges, INRA, UMR 1061, Unite Genet Mol Anim, Limoges, France
[2] INRA, UMR 1313, Unite Genet Anim & Biol Integrat, Jouy En Josas, France
来源
PLOS ONE | 2014年 / 9卷 / 05期
关键词
SKELETAL-MUSCLE MASS; MYOSTATIN GENE; GROWTH; MICE; EXPRESSION; SERUM; MYOD; LOOP;
D O I
10.1371/journal.pone.0097399
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Myostatin is essential for proper regulation of myogenesis, and inactivation of Myostatin results in muscle hypertrophy. Here, we identified an unexpected mutation in the myostatin gene which is almost fixed in Blonde d'Aquitaine cattle. In skeletal muscle, the mutant allele was highly expressed leading to an abnormal transcript consisting of a 41-bp inclusion and premature termination codons and to residual levels of a correctly spliced transcript. This expression pattern, caused by a leaky intronic mutation with regard to spliceosome activity and its apparent stability with regard to surveillance mechanisms, could contribute to the moderate muscle hypertrophy in this cattle breed. This finding is of importance for genetic counseling for meat quantity and quality in livestock production and possibly to manipulate myostatin pre-mRNA in human muscle diseases.
引用
收藏
页数:8
相关论文
共 50 条
  • [31] HPRT DEFICIENCY: IDENTIFICATION OF TWENTY FOUR NOVEL VARIANTS INCLUDING AN UNUSUAL DEEP INTRONIC MUTATION
    Fairbanks, L.
    Corrigan, A.
    Arenas, M.
    Escuredo, E.
    Marinaki, A.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2011, 34 : S249 - S249
  • [32] Non-sense mutation in exon two of the dystrophin gene results in mild Becker muscular dystrophy with generalized muscle hypertrophy
    Witting, N.
    Duno, M.
    Vissing, J.
    NEUROMUSCULAR DISORDERS, 2012, 22 (9-10) : 836 - 836
  • [33] Novel 3698delA mutation in Exon 26 of the dystrophin gene causing Duchenne muscular dystrophy
    Agarwal-Mawal, A
    Vanasse, M
    Simard, LR
    HUMAN MUTATION, 1998, : S23 - S24
  • [34] Case report: a novel deep intronic splice-altering variant in DMD as a cause of Becker muscular dystrophy
    Berntsson, Shala Ghaderi
    Matsson, Hans
    Kristoffersson, Anna
    Niemela, Valter
    van Duyvenvoorde, Hermine A.
    Richel-van Assenbergh, Cindy
    van der Klift, Heleen M.
    Casar-Borota, Olivera
    Frykholm, Carina
    Landtblom, Anne-Marie
    FRONTIERS IN GENETICS, 2023, 14
  • [35] An in-frame pseudoexon activation caused by a novel deep-intronic variant in the dysferlin gene
    Sun, Chengyue
    Xie, Zhiying
    Cong, Lu
    Xu, Yan
    Liu, Zunjing
    ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 2023, 10 (02): : 292 - 296
  • [36] A novel deep intronic MFN2 mutation in a patient with autosomal recessive CMT2.
    van Heurck, Roxane
    Frio, Thomas Rio
    Marconi, Caterina
    Vannier, Anne
    Blouin, Jean-Louis
    Boukrid, Iman
    Fluss, Joel
    Abramowicz, Marc
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1528 - 1528
  • [37] HPRT DEFICIENCY: IDENTIFICATION OF TWENTY-FOUR NOVEL VARIANTS INCLUDING AN UNUSUAL DEEP INTRONIC MUTATION
    Corrigan, A.
    Arenas, M.
    Escuredo, E.
    Fairbanks, L.
    Marinaki, A.
    NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, 2011, 30 (12): : 1260 - 1265
  • [38] A novel single-base mutation mimicking exon deletion of MLPA in symptomatic Duchenne muscular dystrophy carrier
    Cho, Min-Sub
    Lee, Jong-Mok
    ACTA NEUROLOGICA BELGICA, 2021, 121 (01) : 287 - 289
  • [39] A novel single-base mutation mimicking exon deletion of MLPA in symptomatic Duchenne muscular dystrophy carrier
    Min-Sub Cho
    Jong-Mok Lee
    Acta Neurologica Belgica, 2021, 121 : 287 - 289
  • [40] Identification of a Novel Deep Intronic Mutation in CAPN3 Presenting a Promising Target for Therapeutic Splice Modulation
    Hu, Ying
    Mohassel, Payam
    Donkervoort, Sandra
    Yun, Pomi
    Bolduc, Veronique
    Ezzo, Daniel
    Dastgir, Jahannaz
    Marshall, Jamie L.
    Lek, Monkol
    MacArthur, Daniel G.
    Foley, A. Reghan
    Bonnemann, Carsten G.
    JOURNAL OF NEUROMUSCULAR DISEASES, 2019, 6 (04) : 475 - 483