One amino acid drives the lipid droplet targeting sequence of a new noncoding RNA‐encoded protein to mitochondrion

Author:

Yuan Quan1,Zheng Kaixuan2,Huang Ting3,Zhi Zelun4,Xu Yilu1,Cui Liujuan4,Liu Pingsheng24ORCID,Zhang Shuyan4567ORCID

Affiliation:

1. School of Basic Medical Sciences Southwest Medical University Luzhou China

2. University of Chinese Academy of Sciences Beijing China

3. Tianjin Key Laboratory of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine Peking Union Medical College and Chinese Academy of Medical Science Tianjin China

4. Institute of Biophysics Chinese Academy of Sciences Beijing China

5. Beijing Key Laboratory of Emerging Infectious Diseases Institute of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University Beijing China

6. Beijing Institute of Infectious Diseases Beijing China

7. National Center for Infectious Diseases Beijing Ditan Hospital Capital Medical University Beijing China

Abstract

AbstractOver the past decade, the majority of the mammalian genome considered to be noncoding has been revealed to be able to produce proteins. Many RNA molecules, mis‐annotated as noncoding, actually are predicted to code for proteins. Some of those proteins have been identified and verified to play critical roles in multiple biological processes. The lipid droplet (LD) is a unique cellular organelle bound with a phospholipid monolayer membrane, and is closely associated with cellular lipid metabolism and metabolic disorders. However, it is still unclear how a protein targets to LDs. Here we identified a new protein on LDs, LDANP2, which is encoded by noncoding RNA, through a proteomics‐based strategy. The key sequence for its localization on LDs, Truncation 3, is predicted to form an amphipathic helix. Surprisingly, the deletion of the first amino acid in Truncation 3 resulted in mitochondrial localization. How the types of amino acids would determine the LD or mitochondrial localizations of the protein was studied. The findings introduce a useful strategy to mine for new proteins and would provide clues to the understanding of how a protein would find its right organelle, with phospholipid monolayer or bilayer membrane.

Funder

National Natural Science Foundation of China

Ministry of Science and Technology of the People's Republic of China

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

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