ライフサイエンスコーパス: direct repeat

1 r genome is 46,214 bp with a 237 bp terminal direct repeat.

2 the 10 loci contained exact integers of the direct repeat.

3 vealed a tandem PhoP dimer that bound to the direct repeat.

4 occurred at position 6488 generating a 3 bp direct repeat.

5 egion flanked at each terminus by a sizeable direct repeat.

6 lpha binding element (EBE) consists of three direct repeats.

7 two GATA-binding motifs and three octameric direct repeats.

8 typically consist of a tandem arrangement of direct repeats.

9 l peptides, conserved cysteine positions and direct repeats.

10 instability of DNA segments flanked by short direct repeats.

11 mino-acid (aa) direct repeats, and two 88-aa direct repeats.

12 scription by binding in tandem to target DNA direct repeats.

13 displays a 4977-bp deletion flanked by short direct repeats.

14 containing small palindromes embedded within direct repeats.

15 ying genes of unknown function surrounded by direct repeats.

16 and most of these elements are organized as direct repeats.

17 p single deletion in mtDNA, without flanking direct repeats.

18 degree of specificity is associated with the direct repeats.

19 t to a series of non-homologous short (6 bp) direct repeats.

20 flanked on either side by 3.73-kb identical direct repeats.

21 te is located) adjacent to a series of short direct repeats.

22 rspersed repeats that bear both inverted and direct repeats.

23 from cut sites within, or adjacent to, short direct repeats.

24 e half sites that constitute the overlapping direct repeat 1 (DR1) and direct repeat 2 (DR2) motifs a

25 templates for these template switches, with direct repeat 1 (DR1) and DR2 for primer translocation a

26 cleavage generates the plus-strand primer at direct repeat 1 (DR1).

27 binding to the PPAR response element, called direct repeat 1 (DR1).

28 eceptor half sites spaced by one nucleotide (direct repeat 1 [DR1]).

29 end of the minus-strand DNA overlapping the direct repeat 1 in avihepadnaviruses.

30 tes proopiomelanocortin through binding of a direct repeat 1 response element in the promoter, and th

31 y shift assay shows that TR4 can bind to the direct repeat 1 sequence element (AGGTTAAAGGTCT, nucleot

32 initiate plus-strand DNA synthesis from the direct repeat 2 (DR2) located near the opposite end of t

33 te the overlapping direct repeat 1 (DR1) and direct repeat 2 (DR2) motifs and two forkhead factor bin

34 DNA, most of which is in close proximity to direct repeat 2 (DR2); (iii) DP-rcDNA exhibits an RNA pr

35 omni immunoglobulin-binding protein A (IbpA) direct repeat 2 Fic domain (DR2/Fic) for natural host ta

36 sequence (174,601 bp) flanked by a terminal direct repeat (2,910 bp).

37 vated the human ABCA1 promoter, via the same direct repeat 4 (DR4) promoter element as LXR/RXR.

38 ated by a 4-nucleotide spacer similar to the direct repeat 4 element and is designated as a putative

39 receptor/retinoid X receptor (LXR/RXR) on a direct repeat 4 element in the CETP promoter.

40 ponse GADD45beta gene by binding to a distal direct repeat 4 site of the GADD45beta promoter.

41 X receptor (RXR) or CAR-RXR heterodimers to direct repeat-4 type nuclear receptor-binding sites foun

42 via RA receptor beta (RARbeta) binding to a direct repeat 5 (DR5) motif.

43 e mature dorsal spinal cord, expression of a direct repeat 5 RA response element (DR5-RARE) transgene

44 site (TSS) identified 3 conserved hexameric direct repeat-5 elements, RARE1, -2 and -3, and a half s

45 w that the transposon is flanked by an 18-bp direct repeat, a copy of which is also present at the ta

46 efore these deletions, were flanked by short direct repeats, a unique signature of intrachromosomal i

47 These sequences are arranged as direct repeats, an arrangement that can be recognized by

48 xclusively A+T-containing segment, five 9-bp direct repeats, an inverted repeat, and a sigma(A)-depen

49 we created plasmid x chromosome, chromosomal direct repeat and allelic recombination substrates in wh

50 in intergenic regions and RNAs from the long direct repeat and hok/sok elements.

51 NA packaging (pac) site containing two 21-bp direct repeats and a major terminase cleavage site in th

52 While direct repeats and imperfectly homologous sequences appe

53 mes is due primarily to the transposition of direct repeats and insertion sequence (IS) elements.

54 ICE6013 is flanked by 3-bp direct repeats and is demarcated by 8-bp imperfect inver

55 4-bp region containing the deletion had four direct repeats and one inverted repeat.

56 surrounding the deletion contained two 4-bp direct repeats and that a hairpin structure could be for

57 motifs, inverted repeats, mirror repeats and direct repeats and their associated subsets of cruciform

58 ents can insert into genes as closely spaced direct repeats and they frequently undergo incomplete ex

59 Perfect direct repeats and, in particular, the prominent 13 bp r

60 Comparative analysis suggests that a short direct repeat, and a secondary structure including the t

61 R) as scored using a reporter that harbors a direct repeat, and are prone to gross chromosomal rearra

62 ovar Typhimurium strain LT2 was analyzed for direct repeats, and 54 sequences containing variable-num

63 es at a tRNA-methionine locus, is flanked by direct repeats, and encodes a P4-like integrase.

64 spontaneous point mutation, deletion between direct repeats, and intergenomic recombination.

65 ng elements are flanked by either 8- or 9-bp direct repeats, and they differ significantly in size co

66 and cleavage site, three 46-amino-acid (aa) direct repeats, and two 88-aa direct repeats.

67 imilarity); (ii) a central domain containing direct repeats; and (iii) a C-terminal domain that is si

68 erminal inverted repeats, usually flanked by direct repeats; and compared IS-interrupted sequences wi

69 ides an explanation of why both inverted and direct repeats are maintained and how they contribute to

70 Segments flanked by short direct repeats are relatively common in different region

71 s accommodate simultaneous binding of Int to direct-repeat arm sites and indirect-repeat core sites a

72 by recombinational events between nontandem direct repeats as short as 8 bases, and (iii) substituti

73 The presence of A-tails and flanking direct repeats associated with these sequences supported

74 etion inactivated lpr0035, removed the 49-bp direct repeat at the 5' junction of pLP45, and locked pL

75 us type 1 (HSV-1) a sequence is present as a direct repeat at the two termini of the 152-kilobase vir

76 re maintained in all isolates, the number of direct repeats at a locus was polymorphic.

77 The deletions had no or small direct repeats at the breakpoint region.

78 correspondence to the position of two 13-bp direct repeats beginning at nucleotides 8470 and 13 447.

79 ectly bound a region of DNA containing three direct repeats between Pmra and the mraZ gene.

80 ions, each comprised of a novel set of three direct-repeat binding sites spaced 21 bp apart on center

81 A consensus sequence for the two direct repeats bound by HrpY is proposed.

82 deleted, binding was still specific for the direct repeat but was much weaker and appeared to requir

83 eak was made between two copies of a 1290-bp direct repeat by mobilizing a P transposon.

84 with cell source) GC-rich copies of a 102-bp direct repeat (called IR 4) flanked by small unique sequ

85 We show here that transgenes with intrinsic direct repeats can also induce PTGS at a very high frequ

86 HR between linked, direct repeats can occur by gene conversion without an a

87 A single direct-repeat cassette of the element (2x CLE) enhances

88 pes can amplify by unequal exchanges between direct repeats (CD), and both are rare in unselected cul

89 ses its own CRISPR array with short and long direct repeats, cleaves target RNA, and exhibits collate

90 ions, we regularly detected the formation of direct repeats close to the break sites, independent of

91 lA box is 17 nucleotides long and contains a direct repeat comprised of two hexamers separated by 5 n

92 t tcpA, two toxbox elements are present in a direct repeat configuration and both are required for ac

93 ntly, when the RFB is positioned between the direct repeat, conservative gene conversion events predo

94 the nanomolar range, and binds to these two direct repeats cooperatively.

95 strated that COUP-TFII binds to an imperfect direct repeat COUP-TFII recognition sequence (termed her

96 ne conversion and increased both spontaneous direct repeat deletion and spontaneous allelic conversio

97 in vivo trans-complementation assay in which direct repeat deletion through template switching recons

98 ined by using a previously described in vivo direct-repeat deletion assay.

99 cant association of the endpoints with short direct repeats, despite the fact that several such repea

100 repeats, as well as the short host sequence direct repeats diagnostic of insertion.

101 A mutation in the downstream direct repeat DNA sequence allowed high mobility complex

102 Finally, we show that a direct repeat DNA sequence within the hrtAB promoter is

103 s target genes containing two hexanucleotide direct repeat DNA-response elements separated by one bas

104 ange the affinity of AraC for binding to two direct-repeat DNA half-sites.

105 An evolutionarily conserved direct repeat (DR) element, a canonical binding site for

106 s based on target sequences (spacers) in the direct repeat (DR) region (14).

107 nonical inverted repeat was converted into a direct repeat (DR) via large-scale inversion in some Sel

108 CARs are inactive on classical CAR-inducible direct repeat (DR)-4 elements, yet efficiently transacti

109 GTTCA-like direct repeat with a 4 bp spacer [direct repeat (DR)-4)].

110 We report here the generation of a Direct Repeat (DR)-GFP reporter-based mouse model to stu

111 evious report has identified a non-consensus direct repeat (DR-1) element in the RXRgamma2 gene promo

112 ear orphan receptors EAR2 and EAR3 through a direct-repeat (DR) motif.

113 Conserved short direct repeats (DRs), also known as conserved sequences

114 lavivirus genome also contain distinct short direct repeats (DRs), such as RCS3, CS3, RCS2, and CS2.

115 five Rep monomers bind five tetranucleotide direct repeats; each repeat is recognized by two Rep mon

116 definitive, a protein complex that binds to direct repeat elements in the embryonic and fetal beta-t

117 4) were previously shown to bind in vitro to direct repeat elements in the mouse and human embryonic

118 of 220- to 390-nucleotide degenerate tandem direct repeats encoding putative DNA binding proteins.

119 r receptors comprise the DNA-binding core of direct repeat erythroid definitive, a protein complex th

120 ene repressor activity, which we named DRED (direct repeat erythroid-definitive).

121 ng consistency of raw and final data and for directing repeat experiments.

122 Additionally, direct repeats flank two-thirds of the reported mitochon

123 eparated by a coupling sequence derived from direct repeats flanking chromosomal copies of ICEF as a

124 f the element, that corresponded to the 3-bp direct repeats flanking the chromosomal forms.

125 s reports, several of these Ds elements lack direct repeats flanking the deletion junctions and fille

126 -related integration and excision genes, and direct repeats flanking the island, suggest it moves as

127 f conserved sequences, which contained short direct repeats, flanking a variable region.

128 SP-responsive genes were not preceded by the direct repeats found in S. pneumoniae.

129 rm reveals the loss of three of 10 imperfect direct repeats from the central region of the lumenal do

130 ind that pre-crRNAs comprising a full-length direct repeat (full-DR-crRNA) sequence with specific ste

131 The fluorescent yellow direct-repeat (FYDR) mice described here carry two diffe

132 ct or by monomeric DNAs containing a pair of direct repeat GAA.TTC sequences.

133 aliana, was previously shown to contain four direct repeats (Gap boxes, located between -237 and -181

134 by slipped mispairing between 2 copies of a direct repeat (GCGAGCACGAC) separated by 4 bp.

135 ssion of ATPase(-) Rad54 reduced spontaneous direct repeat gene conversion and increased both spontan

136 ing HeLa cell lines harbouring an integrated direct repeat green fluorescent protein reporter for DSB

137 at ComE protects sequences inclusive of both direct repeats, has an equilibrium dissociation constant

138 DNA damage and on both interchromosomal and direct repeat heteroallelic recombination.

139 e, consisting of two motifs of two imperfect direct repeat hexamers spaced by four nucleotides and a

140 nting analysis that includes three imperfect direct repeat hexamers that are needed for full occupanc

141 nting analysis that includes three imperfect direct repeat hexamers.

142 (ssDNA) via a few bases (<5 nt) or extensive direct repeat homologies (>20 nt).

143 es gene expression via binding to the AGGTCA direct repeat hormone response element.

144 Alternatively, direct repeat HR can occur by gene conversion with a cro

145 NA-PKcs on DSB-induced HR, we integrated neo direct repeat HR substrates carrying the I-SceI recognit

146 The element is bordered by two 17-bp direct repeats identical to those found flanking staphyl

147 res the presence of a LytTR family consensus direct repeat in order to stably bind DNA.

148 That H. pylori possesses direct repeats in regions where potential gene rearrange

149 gested that purified ComE binds to two 11-bp direct repeats in the nlmC-comC promoter region, where C

150 ed by DNase I protection assays to a pair of direct repeats in the P2 and P3 promoter regions of the

151 ntly as a monomer to each toxbox in the tcpA direct repeat, in accordance with what we observed previ

152 ISs and their sequence elements-inverted and direct repeats-in raw read data or contigs using flexibl

153 The deleted region, which is flanked by two direct repeats, includes three exons of STX16, the gene

154 ound in the database were flanked by 9-14 bp direct repeats, indicating that their transposition was

155 a primary determinant of PTGS referred to as direct repeat-induced PTGS (driPTGS).

156 oreover, we determined that a minimum of two direct repeats is required to form a stable complex and

157 al sequence composed of four 12-bp imperfect direct repeats (iterons) in the pBtoxis minireplicon was

158 Two 6 bp direct repeats located at the ends of this region appear

159 A spacers interspersed direct repeat locus containing 32 nearly perfect 29-bp r

160 nclude the dnaA-dnaN and NTF regions and the direct repeat locus.

161 due to asymmetric insertion of IS6110 in the direct repeat locus.

162 yping based on the polymorphism in the 36-bp direct-repeat locus was also performed.

163 of toxboxes organized as either inverted or direct repeats may be required for full activation.

164 s in increased mitochondrial frameshifts and direct-repeat mediated deletions but has no effect on th

165 r the first time in mammalian cells, a short direct repeat-mediated noncanonical splicing event induc

166 system to simultaneously monitor spontaneous direct-repeat-mediated deletions (DRMDs) in the nuclear

167 enetic reporter to measure the rate at which direct-repeat-mediated deletions arise in the mitochondr

168 which these deletions arise is unknown, but direct-repeat-mediated deletions involving polymerase sl

169 ast that have an impact on the generation of direct-repeat-mediated deletions.

170 recombination (HR; using fluorescent yellow direct repeat mice), and transcript levels for several r

171 HR in vivo, we have used fluorescent yellow direct repeat mice, in which an HR event at a transgene

172 Meanwhile, two copies of a 146-bp direct repeat motif flanking the deleted region were fou

173 Within the enhancer is a TGACCT direct-repeat motif, required for enhancer activity, tha

174 combinant Ear2 specifically binds the TGACCT direct-repeat motif.

175 es, Xenopus treacle has 11 highly homologous direct repeats near the center of the protein molecule s

176 ected region of 26 to 28 bp encompassing two direct repeats, NTTAAG-n5-WTTAAG, 10 bp upstream of the

177 A direct repeat of 17-24 bases was found on the ends of al

178 he ATPA regulatory element 1 is an imperfect direct repeat of a nuclear receptor response element (A/

179 A direct repeat of an 8-base AU sequence within the 3'-non

180 Hap1 is unusual in binding a direct repeat of CGG triplets, in contacting a TA in the

181 9 proviruses analyzed were flanked by a 6-bp direct repeat of host sequences, as is characteristic fo

182 R64 and R100, which are joined at a 1,953-bp direct repeat of IS100.

183 A perfect direct repeat of the delivered DNA, and inverted and imp

184 odimer, BR-Base-a1-Acid-a1-BR, can bind to a direct repeat of the GCN4 half-site in vivo, leading to

185 A direct repeat of the pentamer GGGGC is present adjacent

186 proximal portion of the enhancer contains a direct repeat of two E-Box motifs, which contributes mos

187 A functional retinoic acid response element direct repeat of two novel motifs separated by a 5-bp sp

188 he enhancer (URE) consisting of three tandem direct repeats of 47 bp.

189 This upstream region contained five direct repeats of 59 base pairs (bp) that increased thym

190 as a highly cooperative dimer by recognizing direct repeats of 7-bp motifs with a 4-bp spacer.

191 C. trachomatis Tarp possesses up to six direct repeats of approximately 50 amino acids each.

192 Direct repeats of Arabidopsis telomeric sequence were co

193 ons are situated within tandem or non-tandem direct repeats of at least 5-bp and may be explained by

194 g analysis revealed that MtrA recognizes two direct repeats of GTCACAgcg-like sequences and that MtrA

195 We found that p53REs are not only direct repeats of half-sites; rather, two p53 half-sites

196 show acts with high efficiency via terminal direct repeats of only 28 bp and with reduced but measur

197 containing the inverted repeat of pAM373 and direct repeats of pAD1 was mobilized efficiently by pAD1

198 silencing induced by a transgene with three direct repeats of the beta-glucuronidase (GUS) open read

199 Synthetic DNA cassettes harboring direct repeats of the CLE motif were placed upstream fro

200 strong TRE consisting of two nearly perfect direct repeats of the consensus nuclear hormone receptor

201 ulated genes have defined canonical RAREs as direct repeats of the consensus RGKTCA separated by 1, 2

202 have recently been identified that resemble direct repeats of the hexameric half-site (ADR3).

203 rom a 2-bp difference between the downstream direct repeats of the P2 and P3 sites.

204 We found that a minimum of three direct repeats of the sequence TTTTGAT is required for T

205 splicing factor composed almost entirely of direct repeats of the tetratricopeptide repeat (TPR) pro

206 opy F'(128) plasmid, where lac is flanked by direct repeats of the transposable element IS3 (1258 bp)

207 bers of nucleotides between distantly spaced direct repeats of three or more base pairs.

208 ty in either assay, either by removal of the direct repeat or by mutation of RAD52, increased the rel

209 pair of repeat tracts where n> or =60 in the direct repeat orientation in vitro.

210 s a pair of ToxT binding sites arranged in a direct repeat orientation upstream of the core promoter

211 a pair of long GAA.TTC repeat tracts in the direct repeat orientation.

212 esent in a single plasmid DNA and are in the direct repeat orientation.

213 usly, one MDS and its outgoing (3') pointer (direct repeat) overlap intron splice sites, indicating t

214 Inverse repeat p53REs favor the H14 mode and direct repeat p53REs may have high possibilities of othe

215 c switch, including PhoP with its associated directed repeat PHO box, candidate motifs for two SARPs,

216 ansversions affecting nucleotides within two direct repeats present in the TcpP-binding region (TGTAA

217 ic homologous recombination between flanking direct repeats, primarily Ty1 elements.

218 o1 promotes replication fork barrier-induced direct repeat recombination but intriguingly limits reco

219 mologue Rqh1 for DNA repair and promotion of direct repeat recombination in the fission yeast Schizos

220 lays a major role in limiting Exo1-dependent direct repeat recombination induced by replication fork

221 Direct repeat recombination induced by ultraviolet light

222 ly unstable and is lost at high frequency by direct repeat recombination involving the loop sequence.

223 We show here for the first time that direct repeat recombination, dependent on Rad22 and Rhp5

224 Rates of mutations, direct repeat recombination, or retrotransposition were

225 fect unequal sister-chromatid recombination, direct-repeat recombination, or mutation.

226 ral genome with a single fully reconstituted direct repeat region (DR) with both terminal cleavage an

227 pacers" separating insertion elements in the direct repeat region of the M. tuberculosis genome.

228 tion may be possible through the inverted or direct repeat regions, while horizontal gene transfer se

229 One mutation defined a cis-acting adjacent direct repeat required for optimal spxB transcription.

230 PAT and kangaroo both contain split direct repeat (SDR) termini, and here we show that DIRS-

231 lindrome separated by 17 bases) and DR-11 (a direct repeat separated by 11 bases) in the 5'-flanking

232 hormone receptor-binding hexad arranged as a direct repeat separated by one nucleotide (DR-1) in the

233 trated that FsrA also binds to two imperfect direct repeats separated by 13 bp, based on the consensu

234 r, conversion frequencies were identical for direct repeats separated by 3800 bp of transcriptionally

235 se proteins generally binds to two imperfect direct repeats separated by a number of bases that place

236 tection region in the P1 promoter contains a direct repeat sequence (GTTAAN(6)GTTAA [where N is any n

237 btr is relieved and Btr binds to a conserved direct repeat sequence adjacent to feuA to activate tran

238 sults, we concluded that SaeR recognizes the direct repeat sequence as a binding site and that bindin

239 DMD methylation is in turn controlled by a direct repeat sequence immediately downstream of the DMD

240 The data also demonstrate that deletion of a direct-repeat sequence restricts the mobility of pLP45 a

241 promoter region containing a 37-bp imperfect direct-repeat sequence.

242 Btr binds to two direct repeat sequences adjacent to the -35 region; reco

243 interaction of TcpP with nucleotides of the direct repeat sequences appears to be a prerequisite for

244 in a manner dependent on the availability of direct repeat sequences in the transgene.

245 on of a double-strand break (DSB) flanked by direct repeat sequences is mediated by single-strand ann

246 s specifically to dsDNA containing the oriT2 direct repeat sequences, confirming their role in transf

247 a short stretches [5-20 nucleotides (nt)] of direct repeat sequences, yielding deletions of interveni

248 ia single-strand annealing of short terminal direct repeats showed substantially higher repair effici

249 rization thus drive Hap1 selectivity for CGG direct repeat sites that contain an asymmetrically posit

250 n many aspects, e.g., having TIR signals and direct repeats, small in size, noncoding, able to fold i

251 ity factor binds in vitro to three imperfect direct repeats, spaced 10 base pairs apart, in a sequent

252 tescibacteria LexA-binding motif has unusual direct-repeat structure, and comparative analyses reveal

253 the saddle-shaped TBP molecule, with its two direct-repeat subdomains and pseudo-two-fold symmetry.

254 quence comprising two loosely conserved 8-bp direct repeat subunits separated by 3 nucleotides.

255 entical inverted repeats and enclosed within direct repeats, suggesting that these genetic regions mi

256 ases) genomes, that have similarly extensive direct repeats, suggests that recombination between such

257 retrotransposons consisting of two terminal direct repeats surrounding a short internal domain.

258 hanisms by which TERT domains and RNA motifs direct repeat synthesis.

259 wo GATA motifs in palindromic (Pal-GATA) and direct-repeat (Tandem-GATA) arrangements, respectively,

260 inding of OmpR family response regulators to direct-repeat targets.

261 of these regions revealed two sets of a TCT direct repeat [TCT-N8-TCT] present at positions (-107 to

262 s terminal inverted repeats (TIRs), terminal direct repeats (TDRs), and interspersed repeats that bea

263 composed of multiple copies of 23-amino-acid direct repeats, termed DR2 and DR1.

264 Trans-splicing of eri-6/7 is mediated by a direct repeat that flanks the eri-6 gene.

265 mutations are associated with palindromic or direct repeats that are either perfect or imperfect.

266 The latter was flanked by inverted/direct repeats that are substrates of SB.

267 It carries 3 tandem direct repeats that comprise 58% of the protein.

268 ers P(RE), P(I), and P(AQ) by binding to two direct repeats that flank the promoter -35 element.

269 donor DNA, deletions of up to 5 kb involving direct repeats that flank the psbA gene were obtained.

270 Recombination between direct repeats that flank the R-M cassette allows for it

271 results in instability of sequences between direct repeats that is dependent on transcription of the

272 by site-specific recombination within 60 bp direct repeats that mark the junctions between ICEBs1 an

273 n size from 81 to 107 bp, and are flanked by direct repeats that vary in length from 6 to 8 bp.

274 rains lacked the missing DNA between the two direct repeats that was found in all large ascospore-der

275 Our results show that MelR binds as a direct repeat to site 2 and site 2' with the C-terminal

276 We showed that MelR binds as a direct repeat to these sites, and we proposed a model to

277 ases has no effect on strand misalignment at direct repeats to produce deletion.

278 oters contain a common regulatory element, a direct repeat typical of OmpR-class transcription factor

279 The aims of this study were to apply direct repeat unit (dru) typing in a large collection of

280 DNA sequence analysis of the direct repeat units within the mec determinant of 30 USA

281 r and that phosphorylated HssR binds to this direct repeat upon exposure of S. aureus to high concent

282 Mutation of this 70-bp UTR and of the direct repeat upregulated both syn and ctr transcription

283 We also identify 38 direct repeat variants that can substitute for the wild-

284 tinylated oligoribonucleotide containing the direct repeat was used as an affinity ligand to purify t

285 recent study, the abundant presence of short direct repeats was documented by comparative bioinformat

286 tion between long CTG.CAG tracts oriented as direct repeats was extraordinarily high; recombinants we

287 d by bacteriophage P1 loxP sites oriented as direct repeats was inserted within a selected gene.

288 The two direct repeats were believed to be responsible for the d

289 he delivered DNA, and inverted and imperfect direct repeats were detected in the same transgene locus

290 uences and status of the 11 bp TIRs and 8-bp direct repeats were determined.

291 Two conserved 7-bp direct repeats were found immediately upstream of the fs

292 Furthermore, similar direct repeats were found upstream of cslAB, comED, comX

293 The P1 phage loxP sites are identical 34-bp direct repeats, whereas the phiC31 phage attB/attP sites

294 of (i) a variable region containing multiple direct repeats which differ in number and sequence from

295 ent PXR DNA-binding motif is the AGTTCA-like direct repeat with a 4 bp spacer [direct repeat (DR)-4)]

296 bsite appears to be oriented as an imperfect direct repeat with its adjacent subsite, although base s

297 heritability, we propose that the intrinsic direct repeat within a transgene may act as a primary de

298 iations resulting from loss or gain of long, direct repeats within the protein coding sequences.

299 in an 11.3-kb segment of DNA flanked by 7-bp direct repeats within the serotype 4 strain which is not

300 iously showed that CpG-rich imperfect tandem direct repeats within three different mouse DMDs (Snurf/