TALE nickase-mediated SP110 knockin endows cattle with increased resistance to tuberculosis

Proc Natl Acad Sci U S A. 2015 Mar 31;112(13):E1530-9. doi: 10.1073/pnas.1421587112. Epub 2015 Mar 2.

Abstract

Transcription activator-like effector nuclease (TALEN)-mediated genome modification has been applied successfully to create transgenic animals in various species, such as mouse, pig, and even monkey. However, transgenic cattle with gene knockin have yet to be created using TALENs. Here, we report site-specific knockin of the transcription activator-like effector (TALE) nickase-mediated SP110 nuclear body protein gene (SP110) via homologous recombination to produce tuberculosis-resistant cattle. In vitro and in vivo challenge and transmission experiments proved that the transgenic cattle are able to control the growth and multiplication of Mycobacterium bovis, turn on the apoptotic pathway of cell death instead of necrosis after infection, and efficiently resist the low dose of M. bovis transmitted from tuberculous cattle in nature. In this study, we developed TALE nickases to modify the genome of Holstein-Friesian cattle, thereby engineering a heritable genome modification that facilitates resistance to tuberculosis.

Keywords: TALEN; disease resistance; homologous recombination; single-strand break; tuberculosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Cattle
  • DNA Breaks, Single-Stranded
  • Deoxyribonuclease I / metabolism*
  • Endonucleases / metabolism
  • Enzyme-Linked Immunospot Assay
  • Female
  • Gene Knock-In Techniques*
  • Gene Transfer Techniques
  • Genome
  • HEK293 Cells
  • Humans
  • Macrophages / microbiology
  • Mice
  • Minor Histocompatibility Antigens
  • Mycobacterium bovis
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / physiology*
  • Transcription, Genetic
  • Tuberculosis, Bovine / genetics*
  • Tuberculosis, Bovine / microbiology
  • Tuberculosis, Bovine / prevention & control*

Substances

  • Minor Histocompatibility Antigens
  • Nuclear Proteins
  • SP110 protein, bovine
  • Sp110 protein, mouse
  • Endonucleases
  • Deoxyribonuclease I