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1 U1 snRNP (U1), in addition to its splicing role, protect
2 U1 snRNP binding to the 5' splice site no. 4 is required
3 U1 snRNP binds to the 5' exon-intron junction of pre-mRN
4 U1 snRNP plays a critical role in 5'-splice site recogni
5 U1 snRNP proteins also contribute to U1 snRNP activity.
6 that this interaction between the galectin-3-U1 snRNP particle and the pre-mRNA results in a producti
7 tract can be reconstituted by the galectin-3-U1 snRNP particle, isolated by immunoprecipitation of th
8 These results indicate that the galectin-3-U1 snRNP-pre-mRNA ternary complex is a functional E comp
9 omplexes, we found this isolated galectin-3--U1 snRNP particle was sufficient to load galectin-3 onto
10 ar ribonucleoprotein (snRNP)-70K (U1-70K), a U1 snRNP-specific protein, is involved in the early stag
11 ein particle (U1 snRNP) 70K (U1-70K) gene, a U1 snRNP-specific protein, has been implicated in basic
12 o show that recombinant yeast U1C protein, a U1 snRNP protein, selects a 5'-splice-site-like sequence
14 y 10S particle that contained galectin-3 and U1 snRNP and this particle was sufficient to load the ga
16 ssociates with RNAP II, and both RNAP II and U1 snRNP are also the most abundant factors associated w
21 the flanking introns allowed normal U2AF and U1 snRNP binding to the target exon splice sites but blo
26 the current model for spliceosome assembly, U1 snRNP binds to the 5' splice site in the E complex fo
27 completely disrupts the association between U1 snRNP and both FUS and RNAP II, but has no effect on
32 in complexes assembled on pre-mRNA, blocking U1 snRNP (small nuclear ribonucleoprotein) binding and e
34 that are needed for maximal binding of both U1 snRNPs and U2 snRNPs to the 5' and 3' splice site, re
35 pon competition with splicing, inhibition by U1 snRNP binding to the intron donor, and the intrinsic
36 e selection of 5'-splice site nucleotides by U1 snRNP is achieved predominantly through basepairing w
37 her reported systems, inhibition of (pA)p by U1 snRNP binding to the intron donor is decreased as the
39 through recognition of the 5' splice site by U1 snRNP and the polypyrimidine tract by the U2 small nu
40 The inhibition of the HIV-1 poly(A) site by U1 snRNP relies on a series of delicately balanced RNA p
44 tiates via formation of a complex comprising U1 snRNP bound at the 5' splice site (5'SS) and the Msl5
48 ings indicate that endogenous RNA-containing U1-snRNP could be a signal that activates the NLRP3 infl
50 to varying degrees and associated with core U1 snRNP proteins to a lesser extent than the canonical
52 2 that are predicted to increase or decrease U1 snRNP binding affinity increase or decrease the usage
54 heir functional antagonism; SF2/ASF enhances U1 snRNP binding at all 5'SSs, the rise in simultaneous
56 To investigate the function of the essential U1 snRNP protein Prp40p, we performed a synthetic lethal
57 ed a novel allele (snu56-2) of the essential U1 snRNP protein Snu56p that exhibits a sporulation defe
59 king an essential canonical splicing factor (U1 snRNP) to this pathway provides strong new evidence t
60 th SL1 is sequence-specific and critical for U1 snRNP biogenesis, further supporting the direct role
61 a critical splicing-independent function for U1 snRNP in protecting the transcriptome, which we propo
63 Our findings underscore a wider role for U1 snRNP in splicing regulation and reveal a novel appro
64 wever, our data also suggest that a site for U1 snRNP binding (e.g., a 5' splice site) within the las
65 wer or increase the affinity of the 5'ss for U1 snRNP result in reduced or increased Vif expression,
67 nucleotide to U1 snRNA to achieve functional U1 snRNP knockdown in HeLa cells, and identified accumul
70 s experiment with U1C isolated from the HeLa U1 snRNP showing that the recombinant U1C is functionall
71 us essential subunits of the yeast and human U1 snRNP, respectively, that are implicated in the estab
78 ese factors transiently associate with human U1 snRNP and are not amenable for structural studies, wh
80 10 in tau pre-mRNA, leading to increases in U1 snRNP binding and in splicing between exon 10 and exo
81 strains depleted of Prp42p formed incomplete U1 snRNPs that failed to produce stable complexes with p
82 (intron-proximal) site, and yet it increases U1 snRNP binding at upstream and downstream sites simult
83 We further demonstrate that RBFOX2 increases U1 snRNP recruitment to the weak 5' splice site through
84 at SEX-LETHAL associates with other integral U1 snRNP components, and we provide genetic evidence to
85 e dose of genes encoding either the integral U1 snRNP protein U1-70k, or the integral U2 snRNP protei
86 well as the potential need for more integral U1-snRNP proteins in governing the fungal 5' splice site
87 structure of U1 snRNP provides insights into U1 snRNP assembly and suggests a possible mechanism of 5
88 operon, and that ribonucleoprotein RNP-2 is U1 snRNP-associated (U1A) whereas RNP-3 is U2 snRNP-asso
92 gest that a U1-PAS axis characterized by low U1 snRNP recognition and a high density of PASs in the u
93 m proteins and U1 snRNA), but not the mature U1 snRNP-specific proteins (U1-70K, U1A and U1C), co-mis
94 Here we report that expression of modified U1 snRNPs with increased affinity to HIV-1 downstream 5'
101 is study, autoantibody recognition of native U1 snRNPs was investigated by dissociating the particle
103 per, we report the identification of a novel U1 snRNP protein, Prp42p, with unexpected properties.
105 inct differences, however, in the ability of U1 snRNP to promote U2 addition, dependent upon its posi
106 'SS occupancy is lower and the affinities of U1 snRNP for the individual sites determine the site of
107 rget TIA-1 and thus increase the affinity of U1 snRNP binding to the intervening donor site, signific
108 We propose that the exclusive association of U1 snRNP/SR proteins with RNAP II positions these splici
111 nd the ability of DISE to promote binding of U1 snRNP, suggested that IAS1 and DISE belong to the sam
112 ion of splicing proteins, and in the case of U1 snRNP we saw reciprocal changes in the levels of U1 s
113 monstrated that U1-70K is a key component of U1 snRNP that mediates inhibition of polyadenylation at
114 ockdown of Gro or snRNP-U1-C (a component of U1 snRNP) showed a significant overlap between genes reg
115 ng protein), hLucA (a potential component of U1 snRNP), and pinin (also called DRS and MemA; a protei
118 ectron density map of the functional core of U1 snRNP at 5.5 A resolution has enabled us to build the
122 ntext, splicing factors acting downstream of U1 snRNP addition bind to a reduced number of ICGs.
123 Possible splicing-independent functions of U1 snRNP-5' splice site interactions during virus replic
124 chemical analyses indicate the importance of U1 snRNP and, to a lesser extent, U6 snRNP in differenti
126 n or antisense oligonucleotide inhibition of U1 snRNP increases the protein level of amyloid precurso
128 obtained when we examined the interaction of U1 snRNP as well as the requirement for SR proteins in c
131 hown by proportionality between the level of U1 snRNP binding to the downstream site and its use in s
132 U1C depletion gives rise to normal levels of U1 snRNP and does not have any detectable effect on U1 s
136 the HMT1 gene deregulates the recruitment of U1 snRNP and its associated components to intron-contain
138 ire linear sequence of the 70-kDa subunit of U1 snRNP (U1-70kDa) small nuclear ribonucleoprotein.
142 E, which is characterized by the presence of U1 snRNPs base-paired to the 5' splice site, components
144 le methods to determine the stoichiometry of U1 snRNPs bound to pre-mRNA with one or two strong 5' sp
150 U1 small nuclear ribonucleoprotein particle (U1 snRNP) 70K (U1-70K) gene, a U1 snRNP-specific protein
151 U1 small nuclear ribonucleoprotein particle (U1 snRNP) 70K protein (U1-70K), one of the three U1 snRN
154 rd of these transcripts, suggesting that PSI-U1 snRNP interactions coordinate the behavioral network
157 Gel mobility shift assays with purified U1 snRNP and oligonucleotide-directed RNase H cleavage e
160 With purified components, hnRNP A1 reduces U1 snRNP binding to 5'SSs by binding cooperatively and i
161 gly, Amin complex formation does not require U1 snRNP or ATP, suggesting that these factors are not n
162 ins with U1 small nuclear ribonucleoprotein (U1 snRNP) binding to the 5' splice site (5'SS), which is
166 with the U1-small nuclear ribonucleoprotein (U1-snRNP) and U3-small nucleolar RNP (snoRNP) in apoptot
167 The U1-small nuclear ribonucleoprotein (U1-snRNP) that includes U1-small nuclear RNA is a highly
168 RNA reduction is the result of sequestration U1 snRNP at levels sufficient to affect splicing and pro
169 between the PSI protein and the spliceosomal U1 snRNP particle is required for normal Drosophila deve
172 st that interaction with the CBC strengthens U1 snRNP binding to the downstream intron donor in a man
175 y complex is a functional E complex and that U1 snRNP is required to assemble galectin-3 onto an acti
180 aining Gems, and motor neurons indicate that U1 snRNP is a component of a molecular pathway associate
183 We further show evidence suggesting that U1 snRNP binds the 5' splice site despite an almost comp
186 he silencing motifs function by altering the U1 snRNP/5' splice site complex in a manner that impairs
190 ive interaction between the pre-mRNA and the U1 snRNP, in which a short RNA duplex is established bet
192 ation by (1) disrupting contacts between the U1 snRNP and the U4/U6-U5 tri-snRNP and (2) orchestratin
195 ain and a U1 recruitment domain, directs the U1 snRNP complex to the terminal exon of a targeted gene
203 ay a key role in RNA splicing by linking the U1 snRNP particle to regulatory RNA-binding proteins.
205 rotein association between components of the U1 snRNP and proteins of the polyadenylation complex.
207 ESE is necessary for the recruitment of the U1 snRNP to the 5' splice site no. 4, even when the 5' s
208 helicase does not affect the loading of the U1 snRNP to the 5'ss during early stage of splicing.
211 rt new synthetic genetic interactions of the U1 snRNP with Msl5 and Mud2 and with the nuclear cap-bin
214 ng cross-intron-bridging interactions of the U1 snRNP*5'SS complex with the Mud2*Msl5*BP complex.
216 eracts with SANS-FILLE in the context of the U1 snRNP, through the characterization of a point mutati
218 s observed with FUS, knockdown of any of the U1 snRNP-specific proteins results in a dramatic loss of
219 nessential splicing factors tested, only the U1 snRNP protein Nam8p is indispensable for Mer1 p-activ
225 x splicing factor required for switching the U1 snRNP with the U6 snRNP at the precursor mRNA (pre-mR
227 rotein protein interactions analogous to the U1 snRNP SF1/BBP U2AF complex that comprises the cross-i
230 the concave surface of tri-snRNP, where the U1 snRNP may reside before its release from the pre-mRNA
231 A comparison of this structure with the U1 snRNP at 5.5 A resolution reveals snRNA-dependent str
233 Moreover, FBP21 interacts directly with the U1 snRNP protein U1C, the core snRNP proteins SmB and Sm
234 in ASF/SF2 enhances its interaction with the U1 snRNP-specific 70K protein and is required for the pr
237 and/or recruitment of these proteins to the U1-snRNP complex is induced by multiple apoptotic stimul
238 e known SRPKs, SRPK1, is associated with the U1-snRNP autoantigen complex in healthy and apoptotic ce
239 ation of phosphorylated SR proteins with the U1-snRNP complex in cells undergoing apoptosis suggests
242 nRNP) 70K protein (U1-70K), one of the three U1 snRNP-specific proteins, is implicated in basic and a
243 licing suggested that factors in addition to U1 snRNP were important for early 5' splice site recogni
246 to splicing, ASF/SF2 can bind selectively to U1 snRNP in an RS domain-dependent, phosphorylation-enha
248 However, although the autoimmune response to U1 snRNPs involves all components of the particle, not a
249 ate that Snu56p interacts with the other two U1 snRNP factors (Mer1p and Nam8p) required for this pro
252 e (herein called a U1 binding site) that via U1 snRNP binding leads to inhibition of the late poly(A)
254 anti-nRNP sera immunoprecipitated U1-C when U1 snRNPs were dissociated before Ab binding, they unexp
255 10S showed an association of galectin-3 with U1 snRNP that was sensitive to treatment with ribonuclea
257 e galectin-3 molecules not in a complex with U1 snRNP (fraction 1 of the same gradient), failed to re
259 e early splicing factor Mud2p functions with U1 snRNP to form a cross-intron bridging complex on nasc
260 ovel SR protein (SR45), which interacts with U1 snRNP 70K protein, a key protein involved in 5' splic
262 tream site, whereas hnRNP A1 interferes with U1 snRNP binding such that 5'SS occupancy is lower and t
264 to process histone RNA and also occurs with U1 snRNPs; therefore, association of SPH1 cannot be cons
267 -protein and RNA-protein interactions within U1 snRNP, and show how the 5' splice site of pre-mRNA is
269 oth required to configure the atypical yeast U1 snRNP into a structure compatible with its evolutiona
270 ere, we report the cryoEM structure of yeast U1 snRNP at 3.6 A resolution with atomic models for ten
274 mirroring yeast Prp42/Prp39, supports yeast U1 snRNP as a model for understanding how transiently as
275 gel electrophoretic assay to find the yeast U1 snRNP in three pre-splicing complexes (delta, beta1,
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