The N-terminus of FILIA forms an atypical KH domain with a unique extension involved in interaction with RNA

PLoS One. 2012;7(1):e30209. doi: 10.1371/journal.pone.0030209. Epub 2012 Jan 19.

Abstract

FILIA is a member of the recently identified oocyte/embryo expressed gene family in eutherian mammals, which is characterized by containing an N-terminal atypical KH domain. Here we report the structure of the N-terminal fragment of FILIA (FILIA-N), which represents the first reported three-dimensional structure of a KH domain in the oocyte/embryo expressed gene family of proteins. The structure of FILIA-N revealed a unique N-terminal extension beyond the canonical KH region, which plays important roles in interaction with RNA. By co-incubation with the lysates of mice ovaries, FILIA and FILIA-N could sequester specific RNA components, supporting the critical roles of FILIA in regulation of RNA transcripts during mouse oogenesis and early embryogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Neoplasm / metabolism
  • Circular Dichroism
  • Crystallography, X-Ray
  • Female
  • Mice
  • Neuro-Oncological Ventral Antigen
  • Ovary / metabolism
  • Poly C / chemistry*
  • Poly U / chemistry*
  • Protein Binding
  • Protein Structure, Tertiary
  • Proteins / chemistry*
  • Proteins / metabolism*
  • RNA / chemistry*
  • RNA / metabolism*
  • RNA-Binding Proteins / metabolism
  • Ultracentrifugation

Substances

  • Antigens, Neoplasm
  • Neuro-Oncological Ventral Antigen
  • Nova2 protein, mouse
  • Proteins
  • RNA-Binding Proteins
  • filia protein, mouse
  • Poly U
  • Poly C
  • RNA

Associated data

  • PDB/3V69