7CGF
Crystal Structure of PUF-8 in Complex with PBE-RNA
Summary for 7CGF
Entry DOI | 10.2210/pdb7cgf/pdb |
Descriptor | PUM-HD domain-containing protein, PBE-5G (5'-R(P*UP*GP*UP*AP*GP*AP*UP*A)-3'), CHLORIDE ION, ... (4 entities in total) |
Functional Keywords | complex, rna binding protein, puf protein |
Biological source | Caenorhabditis elegans More |
Total number of polymer chains | 2 |
Total formula weight | 44492.09 |
Authors | |
Primary citation | Xu, Z.,Zhao, J.,Hong, M.,Zeng, C.,Guang, S.,Shi, Y. Structural recognition of the mRNA 3' UTR by PUF-8 restricts the lifespan of C. elegans. Nucleic Acids Res., 49:10082-10097, 2021 Cited by PubMed Abstract: The molecular mechanisms of aging are unsolved fundamental biological questions. Caenorhabditis elegans is an ideal model organism for investigating aging. PUF-8, a PUF (Pumilio and FBF) protein in C. elegans, is crucial for germline development through binding with the 3' untranslated regions (3' UTR) in the target mRNAs. Recently, PUF-8 was reported to alter mitochondrial dynamics and mitophagy by regulating MFF-1, a mitochondrial fission factor, and subsequently regulated longevity. Here, we determined the crystal structure of the PUF domain of PUF-8 with an RNA substrate. Mutagenesis experiments were performed to alter PUF-8 recognition of its target mRNAs. Those mutations reduced the fertility and extended the lifespan of C. elegans. Deep sequencing of total mRNAs from wild-type and puf-8 mutant worms as well as in vivo RNA Crosslinking and Immunoprecipitation (CLIP) experiments identified six PUF-8 regulated genes, which contain at least one PUF-binding element (PBE) at the 3' UTR. One of the six genes, pqm-1, is crucial for lipid storage and aging process. Knockdown of pqm-1 could revert the lifespan extension of puf-8 mutant animals. We conclude that PUF-8 regulate the lifespan of C. elegans may not only via MFF but also via modulating pqm-1-related pathways. PubMed: 34478557DOI: 10.1093/nar/gkab754 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.7 Å) |
Structure validation
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