Protein & Cell >

2023 , Vol. 14 >Issue 2: 153 - 157

DOI: https://doi.org/10.1093/procel/pwac019

LETTER

A long non-coding RNA LncSync regulates mouse cardiomyocyte homeostasis and cardiac hypertrophy through coordination of miRNA actions

  • Rujin Huang 1,2 ,
  • Jinyang Liu 1 ,
  • Xi Chen 1 ,
  • Ying Zhi 3 ,
  • Shuangyuan Ding 1 ,
  • Jia Ming 1 ,
  • Yulin Li 3 ,
  • Yangming Wang 4 ,
  • Jie Na , 1
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  • 1. Center for Stem Cell Biology and Regenerative Medicine, School of Medicine, Tsinghua University, Beijing 100084, China
  • 2. School of Life Sciences, Tsinghua University, Beijing 100084, China
  • 3. Capital Medical University, Beijing 100084, China
  • 4. Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Peking-Tsinghua Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing 100871, China
jie.na@tsinghua.edu.cn

Accepted date: 26 Apr 2022

Copyright

2022 The Author(s) 2022. Published by Oxford University Press on behalf of Higher Education Press.
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Cite this article

Rujin Huang , Jinyang Liu , Xi Chen , Ying Zhi , Shuangyuan Ding , Jia Ming , Yulin Li , Yangming Wang , Jie Na . A long non-coding RNA LncSync regulates mouse cardiomyocyte homeostasis and cardiac hypertrophy through coordination of miRNA actions[J]. Protein & Cell, 2023 , 14(2) : 153 -157 . DOI: 10.1093/procel/pwac019

References

Publishing order | Descend order by publishing year | Descend order by cited within
1
Agarwal V, Bell GW, Nam JW et al. Predicting effective microRNA target sites in mammalian mRNAs. Elife 2015;4:e0500B.

DOI

2
Betel D, Wilson M, Gabow A et al. The microRNA.org resource: targets and expression. Nucl Acids Res 2008;36:D149–153.

DOI

3
Chen Y, Wang X. miRDB: an online database for prediction of functional microRNA targets. Nucleic Acids Res 2020;48:D127–131.

DOI

4
de Soysa TY, Ranade SS, Okawa S et al. Single-cell analysis of cardiogenesis reveals basis for organ-level developmental defects. Nature 2019;572:120–124.

DOI

5
Ding CC, Rose J, Sun T et al. MESH1 is a cytosolic NADPH phosphatase that regulates ferroptosis. Nat Metab 2020;2:270–277.

DOI

6
Fang X, Wang H, Han D et al. Ferroptosis as a target for protection against cardiomyopathy. Proc Natl Acad Sci USA 2019;116:2672–2680.

DOI

7
Fang X, Cai Z, Wang H et al. Loss of cardiac ferritin H facilitates cardiomyopathy via Slc7a11-mediated ferroptosis. Circ Res 2020;127(4):486–501.

DOI

8
Feng H, Schorpp K, Jin J et al. Transferrin receptor is a specific ferroptosis marker. Cell Rep 2020;30:3411–3423.

DOI

9
George MR, Duan Q, Nagle A et al. Minimal in vivo requirements for developmentally regulated cardiac long intergenic non-coding RNAs. Development 2019;146(23):devl85314.

DOI

10
Han X, Luo S, Peng G et al. Mouse knockout models reveal largely dispensable but context-dependent functions of IncRNAs during development. J Moi Cell Biol 2018;10:175–178.

DOI

11
Haniffa M, Taylor D, Linnarsson S et al. A roadmap for the Human Developmental Cell Atlas. Nature 2021;597:196–205.

DOI

12
Pijuan-Sala B, Griffiths JA, Guibentif C et al. A single-cell molecular map of mouse gastrulation and early organogenesis. Nature 2019;566:490–495.

DOI

13
Shiojima I, Sato K, Izumiya Y et al. Disruption of coordinated cardiac hypertrophy and angiogenesis contributes to the transition to heart failure. J Clin Inuest 2005;115:2108–2118.

DOI

14
Sun X, Sit A, Feinberg MW. Role of miR-181 family in regulating vascular inflammation and immunity. Trends Cardiovasc Med 2014;24:105–112.

DOI

15
Yang WS, SriRamaratnam R, Welsch ME et al. Regulation of ferrop-totic cancer cell death by GPX4. Cell 2014;156:317–331.

DOI

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