6FPP

Structure of S. pombe Mmi1

Summary for 6FPP

• Entry DOI: 10.2210/pdb6fpp/pdb
• Descriptor: YTH domain-containing protein mmi1, GLYCEROL, MAGNESIUM ION, ... (4 entities in total)
• Functional Keywords: meiosis mrna decay, rna binding protein
• Biological source: Schizosaccharomyces pombe (strain 972 / ATCC 24843)
• Total number of polymer chains: 2
• Total formula weight: 37599.09

Authors

Stowell, J.A.W.,Hill, C.H.,Yu, M.,Wagstaff, J.L.,McLaughlin, S.H.,Freund, S.M.V.,Passmore, L.A. (deposition date: 2018-02-11, release date: 2018-05-09, Last modification date: 2024-05-08)

Primary citation

Stowell, J.A.W.,Wagstaff, J.L.,Hill, C.H.,Yu, M.,McLaughlin, S.H.,Freund, S.M.V.,Passmore, L.A.
A low-complexity region in the YTH domain protein Mmi1 enhances RNA binding.
J. Biol. Chem., 293:9210-9222, 2018

PubMed Abstract: Mmi1 is an essential RNA-binding protein in the fission yeast that eliminates meiotic transcripts during normal vegetative growth. Mmi1 contains a YTH domain that binds specific RNA sequences, targeting mRNAs for degradation. The YTH domain of Mmi1 uses a noncanonical RNA-binding surface that includes contacts outside the conserved fold. Here, we report that an N-terminal extension that is proximal to the YTH domain enhances RNA binding. Using X-ray crystallography, NMR, and biophysical methods, we show that this low-complexity region becomes more ordered upon RNA binding. This enhances the affinity of the interaction of the Mmi1 YTH domain with specific RNAs by reducing the dissociation rate of the Mmi1-RNA complex. We propose that the low-complexity region influences RNA binding indirectly by reducing dynamic motions of the RNA-binding groove and stabilizing a conformation of the YTH domain that binds to RNA with high affinity. Taken together, our work reveals how a low-complexity region proximal to a conserved folded domain can adopt an ordered structure to aid nucleic acid binding.

PubMed: 29695507
DOI: 10.1074/jbc.RA118.002291

Experimental method

X-RAY DIFFRACTION (1.93 Å)