LARP1 and LARP4: up close with PABP for mRNA 3' poly(A) protection and stabilization

La-related proteins (LARPs) share a La motif (LaM) followed by an RNA recognition motif (RRM). Together these are termed the La-module that, in the prototypical nuclear La protein and LARP7, mediates binding to the UUU-3MODIFIER LETTER PRIMEOH termination motif of nascent RNA polymerase III transcripts. We briefly review La and LARP7 activities for RNA 3MODIFIER LETTER PRIME end binding and protection from exonucleases before moving to the more recently uncovered poly(A)-related activities of LARP1 and LARP4. Two features shared by LARP1 and LARP4 are direct binding to poly(A) and to the cytoplasmic poly(A)-binding protein (PABP, also known as PABPC1). LARP1, LARP4 and other proteins involved in mRNA translation, deadenylation, and decay, contain PAM2 motifs with variable affinities for the MLLE domain of PABP. We discuss a model in which these PABP-interacting activities contribute to poly(A) pruning of active mRNPs. Evidence that the SARS-CoV-2 RNA virus targets PABP, LARP1, LARP 4 and LARP 4B to control mRNP activity is also briefly reviewed. Recent data suggests that LARP4 opposes deadenylation by stabilizing PABP on mRNA poly(A) tails. Other data suggest that LARP1 can protect mRNA from deadenylation. This is dependent on a PAM2 motif with unique characteristics present in its La-module. Thus, while nuclear La and LARP7 stabilize small RNAs with 3MODIFIER LETTER PRIME oligo(U) from decay, LARP1 and LARP4 bind and protect mRNA 3MODIFIER LETTER PRIME poly(A) tails from deadenylases through close contact with PABP.

Automated summary

La and LARP7 are involved in RNA 3’ end binding and protection, while LARP1 and LARP4 mainly interact with poly(A) and PABP, protecting mRNA poly(A) tails from deadenylases.