The SAMHD1 knockout mouse model: in vivo veritas?

EMBO J. 2013 Sep 11;32(18):2427-9. doi: 10.1038/emboj.2013.190. Epub 2013 Aug 20.

Abstract

EMBO J 32 18, 2454–2462 doi:; DOI: 10.1038/emboj.2013.163; published online July 19 2013

SAMHD1, a dNTP hydrolase mutated in the autoimmune encephalopathy Aicardi-Goutières syndrome, restricts HIV replication in non-dividing human cells by reducing intracellular deoxyribonucleotide pools. New work in The EMBO Journal unexpectedly finds neither autoimmune disease nor increased murine retrovirus infection in SAMHD1 knockout mice, but improved replication of a mutant HIV with increased sensitivity to low dNTP levels. Thus, while the new mouse model partially recapitulates known features of human SAMHD1, it represents a unique tool to study the role of dNTP regulation during inflammation, viral infection and other pathologies.

Publication types

  • Comment

MeSH terms

  • Animals
  • Autoimmune Diseases of the Nervous System / metabolism*
  • HIV Infections / physiopathology*
  • HIV-1 / physiology*
  • Monomeric GTP-Binding Proteins / metabolism*
  • Nervous System Malformations / metabolism*
  • Reverse Transcription / physiology*
  • SAM Domain and HD Domain-Containing Protein 1

Substances

  • SAM Domain and HD Domain-Containing Protein 1
  • Samhd1 protein, mouse
  • Monomeric GTP-Binding Proteins

Supplementary concepts

  • Aicardi-Goutieres syndrome