Formation and removal of 1,N6-dimethyladenosine in mammalian transfer RNA

Author:

You Xue-Jiao123,Zhang Shan12,Chen Juan-Juan2,Tang Feng2,He Jingang45,Wang Jie45,Qi Chu-Bo6,Feng Yu-Qi12ORCID,Yuan Bi-Feng123ORCID

Affiliation:

1. Department of Radiation and Medical Oncology, Cancer Precision Diagnosis and Treatment and Translational Medicine Hubei Engineering Research Center, Zhongnan Hospital of Wuhan University, School of Public Health, Wuhan University , Wuhan  430071,  China

2. Sauvage Center for Molecular Sciences, Department of Chemistry, Wuhan University , Wuhan  430072,  China

3. Wuhan Research Center for Infectious Diseases and Cancer, Chinese Academy of Medical Sciences , Wuhan  430071,  China

4. State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, National Center for Magnetic Resonance in Wuhan, Wuhan Institute of Physics and Mathematics, Innovation Academy for Precision Measurement Science and Technology, Chinese Academy of Sciences-Wuhan National Laboratory for Optoelectronics , Wuhan 430071, China

5. University of Chinese Academy of Sciences ,  Beijing ,  China

6. Department of Pathology, Jiangxi Provincial People's Hospital, The First Affiliated Hospital of Nanchang Medical College , Nanchang 330006, China

Abstract

Abstract RNA molecules harbor diverse modifications that play important regulatory roles in a variety of biological processes. Over 150 modifications have been identified in RNA molecules. N6-methyladenosine (m6A) and 1-methyladenosine (m1A) are prevalent modifications occurring in various RNA species of mammals. Apart from the single methylation of adenosine (m6A and m1A), dual methylation modification occurring in the nucleobase of adenosine, such as N6,N6-dimethyladenosine (m6,6A), also has been reported to be present in RNA of mammals. Whether there are other forms of dual methylation modification occurring in the nucleobase of adenosine other than m6,6A remains elusive. Here, we reported the existence of a novel adenosine dual methylation modification, i.e. 1,N6-dimethyladenosine (m1,6A), in tRNAs of living organisms. We confirmed that m1,6A is located at position 58 of tRNAs and is prevalent in mammalian cells and tissues. The measured level of m1,6A ranged from 0.0049% to 0.047% in tRNAs. Furthermore, we demonstrated that TRMT6/61A could catalyze the formation of m1,6A in tRNAs and m1,6A could be demethylated by ALKBH3. Collectively, the discovery of m1,6A expands the diversity of RNA modifications and may elicit a new tRNA modification-mediated gene regulation pathway.

Funder

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Genetics

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