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1 t encoded in a different frame within the P3 cistron.
2 while allowing translation of the downstream cistron.
3 ing translation of the associated downstream cistron.
4 extended to fusion junctions within each alc cistron.
5 6 to transactivate expression of an internal cistron.
6 that represses translation of the downstream cistron.
7 ysis of the bacteriophage Q beta readthrough cistron.
8  447 nucleotides from within the readthrough cistron.
9 es the access of ribosomes to the downstream cistron.
10 nd can represent any region of the ribosomal cistron.
11  activation of translation of the resistance cistron.
12 llow efficient translation of the downstream cistron.
13 ing frame located upstream of the resistance cistron.
14 cistron; and (c) a group I intron in the 43B cistron.
15 s ruled out possible effects of the reporter cistron.
16 omplex during translation of the ermC leader cistron.
17  Gtx or FGF2 5' leaders linked to a reporter cistron.
18 that contains the mir-17-92 microRNA (miRNA) cistron.
19 the ability to support translation of the 3' cistron.
20 16 (VP16) transcription factor as the second cistron.
21 me in which NS2-3 was restored in the second cistron.
22 dependent of the translation of the upstream cistron.
23  if positioned 134 nt upstream of the distal cistron.
24 usability in the forward design of synthetic cistrons.
25 inserted between the upstream and downstream cistrons.
26 ach His-tagged and in separate transcription cistrons.
27 er and that are uncapped or contain multiple cistrons.
28  for polymorphism in the P1, P3, NIa, and CP cistrons.
29 nimal sequence difference was detected among cistrons.
30 mRNA stimulated expression of the downstream cistron 42-fold.
31 TS) that splits the polymerase gene into two cistrons, 43A and 43B, corresponding to N-terminal (gp43
32 ort open reading frame, termed the 5' leader cistron (5'LC), which is 102 bp upstream of the beta2AR
33  the translational operator of the replicase cistron, a 19 nt fragment (TR).
34 ronic mRNAs with the HIS3 gene as the second cistron and 18 random nucleotides in the intercistronic
35 a monocistronic mRNA encoding the downstream cistron and false identification of an IRES.
36 ctor, which has Renilla luciferase as the 5' cistron and firefly luciferase as the 3' cistron, has be
37 anscriptional activation of the entire C19MC cistron and resulted in suppression of EMT associated ge
38  microsomal P450 enzyme encoded by the first cistron and the auxiliary protein NADPH-P450 reductase b
39 Renilla luciferase or the EGFP) as the first cistron and the yeast Gal4/viral protein 16 (VP16) trans
40  that enables activation of the entire C19MC cistron and uncovers its novel role in suppressing EMT g
41 ge genetic engineering projects require more cistrons and consequently more strong and reliable trans
42 HEG) inserted between the IC-UTS and the 43B cistron; and (c) a group I intron in the 43B cistron.
43 hin the intergenic spacer region of the rDNA cistron, approximately 3 kb upstream (5') of the 18S gen
44 bryophyte) chloroplasts, where the first two cistrons are separated by a spacer region to which no si
45 n by WSMV-GFP, suggesting that both of these cistrons are SIE effectors encoded by WSMV.
46 .4 UTR efficiently translated the luciferase cistron as well, demonstrating the presence of an intern
47 e hairpin, inhibits translation of the first cistron but does not inhibit translation of the cistron
48 ORF2) inhibits translation of the downstream cistron by a process that depends on the uORF2 amino aci
49 and translational control strategies for the cistrons contained therein, but with different specifici
50 hus, ribosomes translating the upstream pabB cistron could be capable of reducing TRAP-dependent cont
51 ions that abolished translation of the first cistron did not, however, affect the IRES-mediated trans
52 tron but does not inhibit translation of the cistron downstream of the c-jun 5' UTR.
53                               The downstream cistron encoded a reporter protein (chloramphenicol acet
54 icistronic transcripts in which the upstream cistron encoded PTB or PTB deletion mutants (including a
55                                    The first cistron encodes the well-characterized alpha1A subunit.
56  cap-independent translation of a downstream cistron encoding Firefly luciferase in a dicistronic exp
57 lthough at least one change occurred in each cistron except HC-Pro and P3.
58 ing events that could account for downstream cistron expression.
59 s conserved despite the duplication of the H cistron for both vectors.
60 gh CAT activity was expressed from the first cistron from all of the dicistronic constructs introduce
61  strategy used by viruses to express several cistrons from one mRNA.
62 rying an insertion-deletion mutation in this cistron germinated normally; thus, the role of GrmA in s
63  5' cistron and firefly luciferase as the 3' cistron, has been found to generate spliced transcripts.
64 88-nt 5'-terminal segment of the 738-nt nsp1 cistron in a BCoV defective interfering (DI) RNA.
65 136 CDS supported expression of a downstream cistron in a bicistronic reporter system.
66  that mediates the translation of the second cistron in a dicistronic mRNA in cultured mammalian cell
67 er could enhance the translation of a second cistron in a dicistronic mRNA.
68 oth M2 and M3 were expressed from a separate cistron in a VSV mutant background that readily establis
69 t the efficient translation of a second URA3 cistron in dicistronic mRNAs in S. cerevisiae, thereby c
70  that nsp4 to nsp10/11 functions as a single cistron in negative-strand RNA synthesis and analyze rec
71 smic acid by enzymes encoded in a seven-gene cistron in P. aeruginosa and in other Pseudomonads.
72 zed steps by enzymes encoded in a seven-gene cistron in Pseudomonas and other organisms.
73                 These results identify a new cistron in the MHV replicase gene locus and show that ns
74 translated only the upstream chloramphenicol cistron in transiently transfected mammalian cells.
75 nd polyamines on translation of a downstream cistron in vivo and support the hypothesis that polyamin
76 ses translation of the associated downstream cistron in vivo.
77 nscript cleavage with individually processed cistrons in operons and gene expression regulated by nuc
78  Our results demonstrate that the downstream cistron, in the bicistronic gene, is expressed to a much
79                  Expression of this internal cistron, in the presence of P6, is greatly enhanced by t
80  the IRES-mediated translation of the second cistron, indicating that this IRES-mediated translation
81 ore, transcriptional activation of the C19MC cistron induced the expression of OCT4 and FGF4 and acce
82 ediate positive and negative control of nine cistrons involved in nucleoside catabolism and recycling
83  15q11-q13 and is paternally expressed, each cistron is a candidate for a role in the imprinted Prade
84    We show that the translation of HPV-18 E6 cistron is regulated by the motif ACCaugGCGCG(C/A)UUU su
85 ains indicates that expression of the second cistron is spatially and temporally regulated.
86 ing increase in the translation of the first cistron (luciferase or EGFP) is monitored either by meas
87 activation of the Qbeta coliphage maturation cistron, mediated by the presence of Qbeta replicase.
88 n situ hybridization for miR-517a/c, a C19MC cistron microRNA, in first trimester human placentas dis
89  is not due to readthrough from the upstream cistron, nor is it due to translation of cryptic monocis
90 osome entry site, expression from the distal cistron of a dicistronic mRNA increased as a function of
91       The E.gracilis rpoA gene is the distal cistron of a multigene cluster that includes genes for c
92 ast, the efficient translation of the second cistron of bicistronic mRNAs, directed by two distinct I
93 report an initial characterization of the E1 cistron of HPV type 16 (HPV-16), the most common oncogen
94 nalyzing ribosome stalling at the regulatory cistron of the antibiotic resistance gene ermA, we uncov
95  beta(2)AR upstream peptide of the 5'-leader cistron of the beta(2)AR, and this polymorphism in the b
96 ated repression selectively targets the nirC cistron of the long nirBDC-cysG operon, an observation t
97 nting protein is translated from a different cistron of the same RNA genome; (iii) 3AB is the most li
98  enzyme SP lyase encoded by splB, the second cistron of the splAB operon.
99 on and point mutations was created in the CP cistron of wild-type and/or green fluorescent protein-ta
100 , the presence of the 5'-UTR between the two cistrons of a bicistronic mRNA stimulated expression of
101  but not all copies of the nuclear ribosomal cistrons of an individual organism, and the changing rat
102     The P1, HC-Pro, P3, CI, NIa, NIb, and CP cistrons of LDSI-S10 and each lineage at passages 1, 3,
103 ent-peptide-dependent stalling at the leader cistrons of several inducible antibiotic resistance gene
104                           Transcription from cistrons of the Escherichia coli CytR regulon is activat
105  the uORF represses translation of the HER-2 cistron or of a heterologous reporter gene.
106 1, HC-Pro, P3, 6K1, CI, 6K2, NIa-VPg, or NIb cistrons permitted efficient superinfection by WSMV expr
107 e, petB(fbcB) was split genetically into two cistrons, petB6 and petBIV, which encoded two polypeptid
108  overlap, out of frame, the downstream major cistron, polyamine regulation was abolished.
109 us is made up of two divergently transcribed cistrons, pspF and pspABCDycjXF.
110 ibed spacer region (ITS) of the nuclear rDNA cistron represents the barcoding locus for Fungi.
111 fluorescent proteins as the first and second cistrons, respectively.
112 ection assays, siRNA knockdown of individual cistrons, RT-PCR to detect mRNA encoded by the bicistron
113                       We constructed a three-cistron Sindbis virus that expresses the alpha and beta
114 TR between an RNA hairpin and the luciferase cistron stimulated expression 119-fold.
115  the IRES-mediated translation of downstream cistron, suggesting that the IRES activity requires the
116 ic region increased expression of the second cistron, suggesting that the viral sequence can function
117 g regions or the stop codons of the upstream cistrons tend to be less susceptible to drug-mediated in
118 etic relatives, gene 43 consists of a single cistron that encodes a PolB family (PolB-type) DNA polym
119 uciferase activity generated from the second cistron that was either equivalent or higher than that o
120 (TriMV) encode two independently functioning cistrons that serve as effectors of SIE at the protein b
121   We analyzed the complete nuclear ribosomal cistron, the complete chloroplast genome, a partial mito
122           Among the regions of the ribosomal cistron, the internal transcribed spacer (ITS) region ha
123 e spacer regions of the ribosomal DNA (rDNA) cistron, to test the hypothesis of unequal mutation rate
124 ed over 100-fold-higher levels of downstream cistron translation than did the Renilla open reading fr
125 ative IRESs promote expression of downstream cistrons via splicing rather than internal initiation of
126                     Expression of the second cistron was dependent upon the intercistronic sequences
127 eLa cells, the translation of the downstream cistron was increased by 50-fold, demonstrating that tra
128                                   The second cistron was not expressed in control dicistronic constru
129 , with c-myc 5' UTR inserted between the two cistrons, was transfected into both HepG2 and HeLa cells
130 of this stop codon, coding for a second mini-cistron, we could not identify another start codon for g
131 hree subunits from the nuclear ribosomal RNA cistron were compared together with regions of three rep
132 ognition sites mapped in the lake trout rDNA cistron were used to digest genomic DNA into fragments o
133                        Cells expressing both cistrons were sorted, and sequences recovered from selec
134  the 5.8S gene of the nuclear ribosomal gene cistrons) were aligned, guided by ITS transcript seconda
135 beta-galactosidase (betaGAL) from the second cistron whereas little or no betaGAL was expressed in th
136 assay eliminated translation of the upstream cistron while allowing translation of the downstream cis
137  expression of NS5A alone from an additional cistron within a replicon construct gave greater rescue
138  major differences in the length of the rDNA cistron within individual lake trout, minimal sequence d
139 5A was expressed from an additional upstream cistron within the RNA to be rescued.

 
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