Literature DB >> 28631368

CRISPR/Cas9-mediated loss of FGF5 function increases wool staple length in sheep.

Wen-Rong Li1,2,3, Chen-Xi Liu2,3, Xue-Mei Zhang2,3, Lei Chen2,3, Xin-Rong Peng2,3, San-Gang He2,3, Jia-Peng Lin2,3, Bin Han2,3, Li-Qin Wang2,3, Jun-Cheng Huang2,3, Ming-Jun Liu2,3.   

Abstract

Fibroblast growth factor 5 (FGF5) regulates hair length in humans and a variety of other animals. To investigate whether FGF5 has similar effects in sheep, we used clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated 9 (Cas9) to generate loss-of-function mutations with the FGF5 gene in Chinese Merino sheep. A total of 16 lambs were identified with genetic mutations within the targeting locus: 13 lambs had biallelic modifications and three lambs had monoallelic modifications. Characterization of the modifications revealed that 13 were frameshift mutations that led to premature termination, whereas the other three were in-frame deletions. Thus, CRISPR/Cas9 efficiently generated loss-of-function mutations in the sheep FGF5 gene. We then investigated the effect of loss of FGF5 function on wool traits in 12 lambs and found that wool staple length and stretched length of genetically modified (GM) yearling sheep were significantly longer compared with that of wild-type (WT) control animals. The greasy fleece weight of GM yearling sheep was also significantly greater compared with that of WT sheep. Moreover, the mean fiber diameter in GM sheep showed no significant difference compared with WT sheep, suggesting that the increase in greasy fleece weight was likely attributed to the increase in wool length. The results of this study suggest that CRISPR/Cas9-mediated loss of FGF5 activity could promote wool growth and, consequently, increase wool length and yield.
© 2017 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.

Entities:  

Keywords:  FGF5; Merino sheep; loss-of-function; staple length; wool

Mesh:

Substances:

Year:  2017        PMID: 28631368     DOI: 10.1111/febs.14144

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  16 in total

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Journal:  Sci Rep       Date:  2018-05-16       Impact factor: 4.379

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