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1 veral processing events of the polycistronic rRNA precursor.
2 find that ZTREs are clustered within the 45S rRNA precursor.
3 ce correlated with that of the extended 4.5S rRNA precursor.
4  site was mapped to the 5' region of the 16S rRNA precursor.
5  YbeY results in the accumulation of the 17S rRNA precursor.
6 subunit by modulating processing of the 15 S rRNA precursor.
7 and it interferes with the degradation of an rRNA precursor.
8  the self-splicing group I intron in the LSU rRNA precursor.
9 splicing group I intron in its large subunit rRNA precursor.
10 nucleoprotein particles that contain the 32S rRNA precursor.
11 egradation of the newly synthesized 5.8S/28S rRNA precursors.
12  northern analysis of steady state levels of rRNA precursors.
13 ays to coordinate the processing of tRNA and rRNA precursors.
14 r rRNA precursors and a depletion of smaller rRNA precursors.
15 -canonical NAD+ cap and maturation of fungal rRNA precursors.
16 The resulting accumulation of ribosomal RNA (rRNA) precursor-analyzed by RNA fluorescent in situ hybr
17  display cell cycle G1 delay and reduced 47S rRNA precursor and 28S rRNA at baseline and serum-challe
18 ation of polyadenylated fragments of the 27S rRNA precursor and that defects in the nuclear exoribonu
19 cessing steps, including a buildup of larger rRNA precursors and a depletion of smaller rRNA precurso
20 ffected cell growth, causing accumulation of rRNA precursors and an aberrant ribosome profile that wa
21 NA (rRNA) processing and preventing aberrant rRNA precursors and discarded fragment accumulation.
22  that functions both in 3'-to-5' trimming of rRNA precursors and in 3'-to-5' degradation of mRNA.
23  to direct sequence-specific modification of rRNA precursors and other nucleolar RNA targets.
24 cked 18 S rRNA formation, increased the 20 S rRNA precursor, and decreased 36 S pre-rRNA, indicating
25 ganization, overaccumulation of 5.8S and 18S rRNA precursors, and an imbalanced 40S:60S ribosome subu
26 epleted of Rps0 protein that contain the 20S rRNA precursor are preferentially excluded from polysome
27                                              rRNA precursors are bound throughout their length by spe
28 ures associated with the Aquifex 16S and 23S rRNA precursors are cleaved at sites that are consistent
29 assembled through a complex process in which rRNA precursors are processed and ribosomal proteins are
30 oRNA-assisted processing of the 5.8S and 28S rRNA precursors, are observed only in metazoan cells.
31  An absB mutation caused accumulation of 30S rRNA precursors, as had previously been reported for E.
32 luding tRNA precursors for RNase P and 5.8 S rRNA precursors, as well as some mRNAs, for RNase MRP.
33 anscription/processing of the ribosomal RNA (rRNA) precursor, as part of ribosome biosynthesis, is in
34 ides trans-splice to a truncated form of the rRNA precursor, but do not compete with cis-splicing whe
35 ems 1, 3, and 4, which may tether U17 to the rRNA precursor by base pairing.
36 B) is known to inhibit cleavage of bacterial rRNA precursors by Escherichia coli ribonuclease III, a
37     The 3' extensions of the accumulating 5S rRNA precursors can be efficiently removed in vitro by p
38 essing, resulting in accumulation of 35S pre-rRNA precursor, formation of a 23S aberrant pre-rRNA, de
39 mall subunit biogenesis by releasing the 18S rRNA precursor from the pre-rRNA.
40 ns-splicing of 5' exon mimics to a truncated rRNA precursor, however, indicate that thio substitution
41 of Mybbp1a results in an accumulation of the rRNA precursor in vivo but surprisingly also causes grow
42           The level of newly synthesized 16S rRNA precursors in R. prowazekii, as analyzed by ribonuc
43           The chemical half-lives of the 16S rRNA precursors in the methionine-starved rickettsiae di
44 f RNase J1 results in an accumulation of 16S rRNA precursors in vivo.
45 hat stabilization of aberrant ribosomal RNA (rRNA) precursors in an enp1-1 mutant causes phenotypes s
46                                      The 45S rRNA precursor is subsequently processed into the mature
47                 Processing of ribosomal RNA (rRNA) precursors is an important component of RNA metabo
48 cause the Ro protein also binds misfolded 5S rRNA precursors, it is proposed to function in a quality
49 ng, the binding sites of AATF within the 45S rRNA precursor localize in close proximity to the SSU cl
50  in situ hybridization on both ribosomes and rRNA precursor molecules as well as in vitro splicing ex
51  been proposed to function in the folding of rRNA precursor molecules.
52 by the severe defects in cleavage of pre-18S rRNA precursors observed upon depletion of the U3 RNA an
53                                      The LSU rRNA precursor of P. carinii contains a conserved group
54 roup I intron (NanGIR2) in the small subunit rRNA precursor of the protist Naegleria andersoni.
55 to 90S preribosomal particles containing 35S rRNA precursor (pre-rRNA).
56 rocessing, including accumulation of the 35S rRNA precursor, presence of a 23S aberrant precursor, de
57 s in MTG3 cause the accumulation of the 15 S rRNA precursor, previously shown to have an 80-nucleotid
58 ouridine modification and normal kinetics of rRNA precursor processing, in contrast with phenotypes r
59 bosomal particles) containing ribosomal RNA (rRNA) precursors, ribosomal proteins (RPs) and a plethor
60                                      The 16S rRNA precursor seems to be identical in size to that acc
61              This pattern of accumulation of rRNA precursors suggests that Mpp10p is required for cle
62                 We have identified a pre-16S rRNA precursor that accumulates in the S. meliloti Delta
63 riptional unit encoding a 45S ribosomal RNA (rRNA) precursor that is then processed to yield the matu
64 s are required for the processing of the 20S rRNA-precursor to mature 18S rRNA, a late step in the ma
65 S pre-rRNA and depletes 20S, 27S, and 7S pre-rRNAs, precursors to the small- and large-subunit rRNAs.
66 s interact with the intervening sequences of rRNA precursor, whereas the others only guide rRNA modif
67 w accumulation of ribosomal subunits and 16S rRNA precursor with a significantly reduced polysome pro