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1 r MSCI-mediated transcriptional silencing of Rpl10.
2  rearrangements controlling the insertion of Rpl10.
3 elix 95 region being adjacent to the protein Rpl10.
4 nexpected and may suggest a nuclear role for Rpl10.
5 tically, rs26802900 is a significant eQTL of RPL10.
6 ty with the gene for human ribosomal protein RPL10.
7  chemoproteomics, we validate that 1 engages RPL10.
8 PL10s differentially contribute to the total RPL10 activity in the male gametophyte.
9 understand the molecular interaction between Rpl10 and Nmd3.
10    Here, we show that cysteines in Rps26 and Rpl10 are readily oxidized, rendering the proteins non-f
11                           Oxidized Rps26 and Rpl10 are released from ribosomes by their chaperones, T
12 8) ) in a high gene density region including RPL10, ATP6A1, FAM50A, and PLXNA3.
13                                        Yeast Rpl10 belongs to the L10e family of ribosomal proteins.
14                         Mutations in LSG1 or RPL10 blocked Nmd3-GFP shuttling into the nucleus and ex
15 ion of RPL10L prevents the death of cultured RPL10-deficient somatic cells, and Rpl10l-promoter-drive
16 ression quantitative locus (eQTL) regulating RPL10 expression in the putamen and other brain tissues
17 ated that Arabidopsis (Arabidopsis thaliana) RPL10 genes are involved in development and translation
18 tions in the nucleus have been described for RPL10 in different organisms.
19 10l-promoter-driven transgenic expression of Rpl10 in spermatocytes restores spermatogenesis and fert
20 ating intersubunit rotation originating from rpL10 in the core of the large subunit (LSU) through bot
21 oop in the essential yeast ribosomal protein rpL10 is a central controller of this process.
22                 In the large (60 S) subunit, Rpl10 is positioned in a cleft between the central protu
23                We have shown previously that Rpl10 is required for the release of the Crm1-dependent
24                   The RIBOSOMAL PROTEIN L10 (RPL10) is an integral component of the eukaryotic riboso
25 es transcription of a ribosomal protein L10 (Rpl10)-like gene and the cell cycle inhibitor p27, and i
26                                          The rpL10 loop is also involved in Sdo1p recruitment, sugges
27 tural and biochemical effects, suppressed an rpL10 mutant, re-establishing rotational equilibrium.
28 e three AtRPL10 genes can complement a yeast RPL10 mutant.
29     Moreover, the characterization of double rpl10 mutants indicates that the three AtRPL10s differen
30 ing that the block in 60S export in lsg1 and rpl10 mutants results indirectly from failing to recycle
31 and the block in 60S export in both lsg1 and rpl10 mutants was also suppressed by mutant Nmd3 protein
32 ystal and solution structures of prokaryotic Rpl10 orthologs.
33 the dominant LSG1 mutant also traps a mutant Rpl10 protein that does not normally bind stably to the
34 new evidence about the nonredundant roles of RPL10 proteins in Arabidopsis.
35                    We also found that mutant Rpl10 proteins were engineered to be unable to bind to t
36  (PDS) or a ribosomal protein-encoding gene, RPL10 (QM), in Nicotiana benthamiana We analyzed the exp
37     Here, this paradox is explored using the rpL10-R98S (uL16-R98S) mutant yeast model of the most co
38                              The presence of RPL10-R98S and other RP mutations also correlated with a
39 ion of NOTCH1 eliminated these phenotypes in RPL10-R98S cells, in part via downregulation of PKC-thet
40 roliferation defect is eventually rescued by RPL10-R98S mouse lymphoid cells that acquire 5-fold more
41 ous cancer types, for example, the recurrent RPL10-R98S mutation in T-cell acute lymphoblastic leukem
42                    We previously showed that RPL10-R98S promotes expression of oncogenes, but also in
43                                              RPL10-R98S-associated cellular oxidative stress promoted
44        In this paper, we show that a loop of Rpl10 that embraces the P-site transfer ribonucleic acid
45 ried out an extensive mutational analysis of Rpl10 to identify mutations that would allow us to map a
46 nd translocation of the downstream component RPL10 to the nucleus, where it interacts with a newly id
47 oplasm by insertion of the ribosomal protein Rpl10 (uL16).
48 pl10l expression compensates for the lack of Rpl10, which exhibits a broad expression pattern but is
49 y of Rpl10l, a murine autosomal retrogene of Rpl10 with testis-specific expression, disturbs ribosome
50 p is not necessary for stable interaction of Rpl10 with the ribosome, suggesting that it plays a dyna
51 wnregulation of PKC-theta, with no effect on RPL10-WT cells.
52 acquire 5-fold more secondary mutations than RPL10-WT cells.