Talin rod domain-containing protein 1 (TLNRD1) is a novel actin-bundling protein which promotes filopodia formation

J Cell Biol. 2021 Sep 6;220(9):e202005214. doi: 10.1083/jcb.202005214. Epub 2021 Jul 15.

Abstract

Talin is a mechanosensitive adapter protein that couples integrins to the cytoskeleton. Talin rod domain-containing protein 1 (TLNRD1) shares 22% homology with the talin R7R8 rod domains, and is highly conserved throughout vertebrate evolution, although little is known about its function. Here we show that TLNRD1 is an α-helical protein structurally homologous to talin R7R8. Like talin R7R8, TLNRD1 binds F-actin, but because it forms a novel antiparallel dimer, it also bundles F-actin. In addition, it binds the same LD motif-containing proteins, RIAM and KANK, as talin R7R8. In cells, TLNRD1 localizes to actin bundles as well as to filopodia. Increasing TLNRD1 expression enhances filopodia formation and cell migration on 2D substrates, while TLNRD1 down-regulation has the opposite effect. Together, our results suggest that TLNRD1 has retained the diverse interactions of talin R7R8, but has developed distinct functionality as an actin-bundling protein that promotes filopodia assembly.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / metabolism*
  • Actin Cytoskeleton / ultrastructure
  • Actins / genetics
  • Actins / metabolism*
  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Amino Acid Sequence
  • Binding Sites
  • Cell Line, Tumor
  • Cell Movement
  • Cloning, Molecular
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Gene Expression
  • Gene Expression Regulation
  • Genetic Vectors / chemistry
  • Genetic Vectors / metabolism
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Models, Molecular
  • Molecular Chaperones / antagonists & inhibitors
  • Molecular Chaperones / chemistry
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism*
  • Osteoblasts / cytology
  • Osteoblasts / metabolism
  • Protein Binding
  • Protein Conformation, alpha-Helical
  • Protein Multimerization
  • Pseudopodia / metabolism*
  • Pseudopodia / ultrastructure
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Signal Transduction
  • Talin / genetics
  • Talin / metabolism*

Substances

  • APBB1IP protein, human
  • Actins
  • Adaptor Proteins, Signal Transducing
  • Cytoskeletal Proteins
  • KANK1 protein, human
  • Membrane Proteins
  • Molecular Chaperones
  • RNA, Small Interfering
  • Recombinant Proteins
  • TLNRD1 protein, human
  • Talin