The La-related proteins: structures and interactions of a versatile superfamily of RNA-binding proteins

ABSTRACT

The La-related proteins (LaRPs) are an ancient superfamily of RNA-binding proteins orchestrating the major fates of RNA, from processing and maturation to regulation of mRNA translation. LaRPs are instrumental in modulating complex assemblies where the RNA is bound, folded, processed, escorted and presented to the functional effectors often through recruitment of protein partners. This intricate web of protein-RNA and protein–protein interactions is enabled by the modular nature of the LaRPs, comprising several structured domains connected by flexible linkers, and other sequences lacking recognizable folded motifs. Recent structures, together with biochemical and biophysical studies, have provided insights into how each LaRP family has evolved unique mechanisms of RNA recognition, not only through the conserved RNA-binding unit, the La-module, but also mediated by other family-specific motifs. Furthermore, in a series of unexpected twists and turns, they have revealed that the dynamic and conformational interplay of multi-structured domains and disordered regions operate in unison to achieve RNA substrate discrimination. This review proposes a perspective of our current knowledge of the structure–function relationship of the LaRP superfamily.

KEYWORDS:

• La-related proteins
• LaRP
• RNA-binding proteins
• RNA biology
• La-module
• RRM
• structure-function relationship

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

The authors are grateful for grant support of their work in
this area: MRC (Wellcome Trust, Newton Royal Society Fellowship, ref. [NF140482], EU Horizon 2020 research and innovation programme Marie Sklodowska-Curie fellowship, agreement [655341]); ACDB (Région Bretagne SAD2-2017-RNA2init, SAD17009); KAL (National Institutes of Health – National Institute of General Medical Sciences) [R15GM119096].