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Toll/interleukin-1 receptor (TIR) domain-containing proteins have NAD-RNA decapping activity.
Wang, Xufeng; Yu, Dongli; Yu, Jiancheng; Hu, Hao; Hang, Runlai; Amador, Zachary; Chen, Qi; Chai, Jijie; Chen, Xuemei.
Afiliação
  • Wang X; State Key Laboratory for Protein and Plant Gene Research, Peking-Tsinghua Joint Center for Life Sciences, School of Life Sciences, Peking University, Beijing, 100871, China.
  • Yu D; Beijing Advanced Center of RNA Biology (BEACON), Peking University, Beijing, 100871, China.
  • Yu J; Department of Botany and Plant Sciences, Institute of Integrative Genome Biology, University of California, Riverside, CA, 92521, USA.
  • Hu H; Institute of Biochemistry, University of Cologne, Cologne, 50674, Germany.
  • Hang R; Max Planck Institute for Plant Breeding Research, Cologne, 50829, Germany.
  • Amador Z; Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, 02215, USA.
  • Chen Q; Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT, 84112, USA.
  • Chai J; State Key Laboratory for Protein and Plant Gene Research, Peking-Tsinghua Joint Center for Life Sciences, School of Life Sciences, Peking University, Beijing, 100871, China.
  • Chen X; Beijing Advanced Center of RNA Biology (BEACON), Peking University, Beijing, 100871, China.
Nat Commun ; 15(1): 2261, 2024 Mar 13.
Article em En | MEDLINE | ID: mdl-38480720
ABSTRACT
The occurrence of NAD+ as a non-canonical RNA cap has been demonstrated in diverse organisms. TIR domain-containing proteins present in all kingdoms of life act in defense responses and can have NADase activity that hydrolyzes NAD+. Here, we show that TIR domain-containing proteins from several bacterial and one archaeal species can remove the NAM moiety from NAD-capped RNAs (NAD-RNAs). We demonstrate that the deNAMing activity of AbTir (from Acinetobacter baumannii) on NAD-RNA specifically produces a cyclic ADPR-RNA, which can be further decapped in vitro by known decapping enzymes. Heterologous expression of the wild-type but not a catalytic mutant AbTir in E. coli suppressed cell propagation and reduced the levels of NAD-RNAs from a subset of genes before cellular NAD+ levels are impacted. Collectively, the in vitro and in vivo analyses demonstrate that TIR domain-containing proteins can function as a deNAMing enzyme of NAD-RNAs, raising the possibility of TIR domain proteins acting in gene expression regulation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Escherichia coli / NAD Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Escherichia coli / NAD Idioma: En Ano de publicação: 2024 Tipo de documento: Article