Identification and functional comparison of novel alternatively spliced isoforms of human YAP

Author:

Liu Lianlian12ORCID,Zhang Junlei1ORCID,Wang Jiaqi13,Tian Yanping1,Wang Jiali1,Xu Yixiao1,Cheng Yuda12,Yu Meng14,Wang Jiangjun15,Yang Yi6,Wang Xueyue7,Yang Ran13,Wu Wei8,Zhang Chen1,Hu Yan9,Jian Rui1,Xiao Lan2,Ruan Yan1ORCID

Affiliation:

1. Laboratory of Stem Cell & Developmental Biology, Department of Histology and Embryology Army Medical University Chongqing China

2. Department of Histology and Embryology, Chongqing Key Laboratory of Neurobiology, Brain and Intelligence Research Key Laboratory of Chongqing Education Commission Army Medical University Chongqing China

3. Department of Pathophysiology, College of High Altitude Military Medicine Army Medical University Chongqing China

4. Joint Surgery Center, Southwest Hospital Army Medical University Chongqing China

5. Department of Cell Biology, College of Basic Medicine Army Medical University Chongqing China

6. Experimental Center of Basic Medicine, College of Basic Medical Sciences Army Medical University Chongqing China

7. Department of Pediatrics The General Hospital of PLA Tibet Military Area Command Lhasa China

8. Thoracic Surgery Department Southwest Hospital, The First Hospital Affiliated to Army Medical University Chongqing China

9. Department of Military Basic Training and Army Management, Army Health Service Training Base Army Medical University Chongqing China

Abstract

As a key effector of the Hippo pathway, yes‐associated protein (YAP) is a major regulator of cell proliferation and apoptosis. In this study, 23 hYAP isoforms were identified in HEK293 cells, with 14 isoforms being reported for the first time. These isoforms were classified into hYAP‐a and hYAP‐b isoforms based on the variation in exon 1. The two groups of isoforms showed distinctly different subcellular localizations. hYAP‐a isoforms could activate TEAD‐ or P73‐mediated transcription, affect the proliferation rate, and enhance the cellular chemosensitivity of HEK293 cells. Moreover, different activation abilities and pro‐cytotoxic effects were observed among hYAP‐a isoforms. However, hYAP‐b isoforms were not found to exert any significant biological effects. Our findings add to the knowledge of YAP gene structure and protein‐coding capacity and will help in the elucidation of the function and related molecular mechanisms of the Hippo‐YAP signaling pathway.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Biochemistry, Genetics and Molecular Biology

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