TLN1 contains a cancer-associated cassette exon that alters talin-1 mechanosensitivity

Author:

Gallego-Paez Lina M.1ORCID,Edwards William J.S.2ORCID,Chanduri Manasa3ORCID,Guo Yanyu4ORCID,Koorman Thijs5ORCID,Lee Chieh-Yu1ORCID,Grexa Nina1ORCID,Derksen Patrick5ORCID,Yan Jie46ORCID,Schwartz Martin A.37ORCID,Mauer Jan18ORCID,Goult Benjamin Thomas2ORCID

Affiliation:

1. BioMed X Institute (GmbH) 1 , Heidelberg, Germany

2. School of Biosciences, University of Kent 2 , Canterbury, UK

3. Departments of Internal Medicine (Cardiology) and Yale Cardiovascular Research Center 3 , New Haven, CT, USA

4. Mechanobiology Institute, National University of Singapore 4 , Singapore, Singapore

5. Department of Pathology, University Medical Center Utrecht 5 , Utrecht, Netherlands

6. Department of Physics, National University of Singapore 6 , Singapore, Singapore

7. Departments of Cell Biology and Biomedical Engineering, Yale School of Medicine 7 , New Haven, CT, USA

8. 8Department of Immunology, Novartis Institutes for BioMedical Research, Basel, Switzerland

Abstract

Talin-1 is the core mechanosensitive adapter protein linking integrins to the cytoskeleton. The TLN1 gene is comprised of 57 exons that encode the 2,541 amino acid TLN1 protein. TLN1 was previously considered to be expressed as a single isoform. However, through differential pre-mRNA splicing analysis, we discovered a cancer-enriched, non-annotated 51-nucleotide exon in TLN1 between exons 17 and 18, which we refer to as exon 17b. TLN1 is comprised of an N-terminal FERM domain, linked to 13 force-dependent switch domains, R1-R13. Inclusion of exon 17b introduces an in-frame insertion of 17 amino acids immediately after Gln665 in the region between R1 and R2 which lowers the force required to open the R1-R2 switches potentially altering downstream mechanotransduction. Biochemical analysis of this isoform revealed enhanced vinculin binding, and cells expressing this variant show altered adhesion dynamics and motility. Finally, we showed that the TGF-β/SMAD3 signaling pathway regulates this isoform switch. Future studies will need to consider the balance of these two TLN1 isoforms.

Funder

Biotechnology and Biological Sciences Research Council

Cancer Research UK

Merck KGaA

United States Public Health Service

Ministry of Education

Breast Cancer Now

European Union

European Cooperation in Science and Technology

University of Kent

Publisher

Rockefeller University Press

Subject

Cell Biology

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