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XB-ART-7117
Mol Cell Biol June 1, 2002; 22 (12): 4101-12.
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Xenopus LSm proteins bind U8 snoRNA via an internal evolutionarily conserved octamer sequence.

Tomasevic N , Peculis BA .


Abstract
U8 snoRNA plays a unique role in ribosome biogenesis: it is the only snoRNA essential for maturation of the large ribosomal subunit RNAs, 5.8S and 28S. To learn the mechanisms behind the in vivo role of U8 snoRNA, we have purified to near homogeneity and characterized a set of proteins responsible for the formation of a specific U8 RNA-binding complex. This 75-kDa complex is stable in the absence of added RNA and binds U8 with high specificity, requiring the conserved octamer sequence present in all U8 homologues. At least two proteins in this complex can be cross-linked directly to U8 RNA. We have identified the proteins as Xenopus homologues of the LSm (like Sm) proteins, which were previously reported to be involved in cytoplasmic degradation of mRNA and nuclear stabilization of U6 snRNA. We have identified LSm2, -3, -4, -6, -7, and -8 in our purified complex and found that this complex associates with U8 RNA in vivo. This purified complex can bind U6 snRNA in vitro but does not bind U3 or U14 snoRNA in vitro, demonstrating that the LSm complex specifically recognizes U8 RNA.

PubMed ID: 12024024
PMC ID: PMC133881
Article link: Mol Cell Biol


Species referenced: Xenopus
Genes referenced: lsm2 lsm3 lsm4 lsm6 lsm7 lsm8

References [+] :
Achsel, A doughnut-shaped heteromer of human Sm-like proteins binds to the 3'-end of U6 snRNA, thereby facilitating U4/U6 duplex formation in vitro. 1999, Pubmed