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Free keywords:
snRNA, small nuclear RNA, snRNP, small nuclear ribonucleoprotein, SMN, survival motor neuron, PRMT5, p protein arginine methyltransferase 5, WD45, WD repeat domain 45, pICln, chloride conductance regulatory protein, CBC, cap-binding complex, PHAX, phosphorylated adaptor for RNA export, CRM1, chromosome region maintenance 1, RanGTP, Ras-related nuclear protein bound to GTP,
NPC, nuclear pore complex, Tgs1, trimethylguanosine synthetase1,
NLS, nuclear localization signal, SPN1, snurportin-1, Lsm proteins,
like Sm protein, U snRNP biogenesis, SMN-complex, PRMT5-complex, Sm proteins, Splicing, U snRNA
Abstract:
The assembly of the Sm‐class of uridine‐rich small nuclear ribonucleoproteins (U snRNPs), albeit spontaneous in vitro, has recently been shown to be dependent on the aid of a large number of assisting factors in vivo. These factors are organized in two interacting units termed survival motor neuron (SMN)‐ and protein arginine methyltransferase 5 (PRMT5)‐complexes, respectively. While the PRMT5‐complex acts early in the assembly pathway by activating common proteins of U snRNPs, the SMN‐complex functions to join proteins and RNA in a highly ordered, apparently regulated manner. Here, we summarize recent progress in the understanding of this process and discuss the influence exerted by the aforementioned trans‐acting factors.