ライフサイエンスコーパス: intercistronic

1 ctor, and, intriguingly, we also identify an intercistronic AdoCbl riboswitch that has a predicted st

2 Shorter intercistronic distance is associated with greater use o

3 uORF number, intercistronic distance, overlap with the CDS, and initi

4 the essential features of C.elegans operons: intercistronic distances in the range of 104-257 nt betw

5 ireplicon containing the wild-type or mutant intercistronic gene junctions for the ability to direct

6 The intercistronic gene junctions of vesicular stomatitis vi

7 erminant of transcription termination at the intercistronic gene junctions of VSV.

8 hat assembled on the Cricket paralysis virus intercistronic internal ribosomal entry site (IRES) with

9 family of transcripts is the presence of an intercistronic IRES that we have previously shown to con

10 translation that was transmitted across the intercistronic junction (coupling frequency).

11 plit ribosome binding site at the gene 26-25 intercistronic junction, which is highly competent in th

12 pstream gene interferes with coupling in the intercistronic junction.

13 transcripts and KorB repressor bound to the intercistronic kilB promoter region are important for mo

14 The inhibitory effect of intercistronic located secondary structure on translatio

15 n studies and patterns of high divergence of intercistronic nucleotide sequences of this cluster sugg

16 re much lower than the rate observed for the intercistronic recombination hot spot in BMV RNA3.

17 The IRES was mapped to the intercistronic region (ICR) of a bicistronic mRNA that w

18 The eighth site was within the intercistronic region (ICR) of plus-strand RNA3.

19 e utilization phenotype lay in the abgR-abgA intercistronic region and appeared to allow the expressi

20 increased as a function of the length of the intercistronic region and the concentration of PABP.

21 ment homolog can be recognized in the 240-bp intercistronic region between ctaB and ctaC.

22 It mapped upstream from the intercistronic region containing the gene V stop codon a

23 this method, the presence of an IRES in the intercistronic region facilitates the translation of Gal

24 of the translationally coupled geneV-geneVII intercistronic region from M13 phage.

25 Importantly, a putative intercistronic region from one of these potential enople

26 resence of the TEV 5' leader sequence in the intercistronic region increased expression of the second

27 uced the 5'-UTR of mouse Kv1.4 mRNA into the intercistronic region of a bicistronic vector containing

28 leader, as well as the common exon into the intercistronic region of a dicistronic luciferase constr

29 number of copies of this IRES module in the intercistronic region of a dicistronic mRNA strongly enh

30 otes internal initiation when present in the intercistronic region of a dicistronic mRNA, indicating

31 translation in vivo even when present in the intercistronic region of a discistronic mRNA, indicating

32 ein CUGBP1 and the integrity of the CUG-rich intercistronic region of c/ebpbeta mRNA.

33 Moreover, when tested in the intercistronic region of dicistronic mRNAs, both sequenc

34 y inserting the 5' leader sequences into the intercistronic region of dicistronic mRNAs.

35 Here, we report mutational analysis of the intercistronic region of this operon by linker scan anal

36 ond cistron and 18 random nucleotides in the intercistronic region was introduced into a yeast strain

37 rs MgrA and NorG and shares a 420-nucleotide intercistronic region with the divergently transcribed p

38 -ctaC'-lacZ fusion (containing the ctaB-ctaC intercistronic region) was placed at a remote nonessenti

39 yrP gene encoding a uracil permease, a 13-nt intercistronic region, and the pyrB gene encoding aspart

40 other internal promoter lay in the secG-yvaK intercistronic region, and this activity (P(B)) was depe

41 ate the presence of an extra promoter in the intercistronic region, creating what has been termed a "

42 protein for the operon, a 39-nucleotide (nt) intercistronic region, the pyrP gene encoding a uracil p

43 rter containing the GATA-4 5'-UTR within the intercistronic region, we demonstrate that this leader s

44 iption terminator element located within the intercistronic region.

45 tained random sequences of 9 or 18 nt in the intercistronic region.

46 e 5' leader sequence of the CLN3 mRNA in the intercistronic region.

47 having translated the uORF despite the short intercistronic region.

48 ependent attenuator located in the tyrS-pdxY intercistronic region.

49 licing is exclusively to SL1 and there is no intercistronic region; the polyadenylation signal is onl

50 found at the Shine-Dalgarno sequences and in intercistronic regions are processed with higher efficie

51 Furthermore, this element is predicted in intercistronic regions of numerous operons of C. elegans

52 olytic processing in the 3' untranslated and intercistronic regions, and sites within the coding regi

53 n, are present in the pyrR-pyrP or pyrP-pyrB intercistronic regions.

54 e uORF reinitiate inefficiently and that the intercistronic sequence downstream of the uORF mediates

55 of the second cistron was dependent upon the intercistronic sequences and was indicative of IRES acti

56 Intercistronic sequences recovered from cells that did g

57 The absence of a promoter in the ctaB-ctaC intercistronic space also was indicated by the inability

58 anscripts containing the HCV IRES within the intercistronic space fused to downstream sequence encodi

59 aining 5' nontranslated sequences within the intercistronic space was consistent with the presence of

60 poliovirus IRES which was placed within the intercistronic space.

61 wnstream AUG codon, in part due to the short intercistronic spacing.

62 types of DNA insertion elements: (a) a short intercistronic untranslated sequence (IC-UTS) that split