Sharma Shraddha, Patnaik Santosh K, Taggart R Thomas, Kannisto Eric D, Enriquez Sally M, Gollnick Paul, Baysal Bora E
Department of Pathology, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, New York 14203, USA.
Department of Thoracic Surgery, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, New York 14203, USA.
Nat Commun. 2015 Apr 21;6:6881. doi: 10.1038/ncomms7881.
The extent, regulation and enzymatic basis of RNA editing by cytidine deamination are incompletely understood. Here we show that transcripts of hundreds of genes undergo site-specific C>U RNA editing in macrophages during M1 polarization and in monocytes in response to hypoxia and interferons. This editing alters the amino acid sequences for scores of proteins, including many that are involved in pathogenesis of viral diseases. APOBEC3A, which is known to deaminate cytidines of single-stranded DNA and to inhibit viruses and retrotransposons, mediates this RNA editing. Amino acid residues of APOBEC3A that are known to be required for its DNA deamination and anti-retrotransposition activities were also found to affect its RNA deamination activity. Our study demonstrates the cellular RNA editing activity of a member of the APOBEC3 family of innate restriction factors and expands the understanding of C>U RNA editing in mammals.
胞苷脱氨介导的RNA编辑的范围、调控及酶学基础尚未完全明确。在此,我们发现数百个基因的转录本在M1极化的巨噬细胞中以及在低氧和干扰素刺激下的单核细胞中发生位点特异性C>U RNA编辑。这种编辑改变了许多蛋白质的氨基酸序列,其中包括许多与病毒性疾病发病机制相关的蛋白质。已知可使单链DNA胞苷脱氨并抑制病毒和逆转录转座子的载脂蛋白B mRNA编辑酶催化多肽样3A(APOBEC3A)介导了这种RNA编辑。我们还发现,已知的APOBEC3A参与DNA脱氨和抗逆转录转座活性所需的氨基酸残基也会影响其RNA脱氨活性。我们的研究证明了先天限制因子APOBEC3家族成员的细胞RNA编辑活性,并扩展了对哺乳动物中C>U RNA编辑的认识。