ライフサイエンスコーパス: insertion sequence

1 high levels as a result of a third mutation (insertion sequence).

2 ix domain, and a transmembrane and cytosolic insertion sequence.

3 f an internal 57-amino-acid-long hydrophobic insertion sequence.

4 when there are fewer than five copies of the insertion sequence.

5 with olefins via a C-H activation, migratory insertion sequence.

6 /- 31 900 different, EpiSC-specific, peptide insertion sequences.

7 ene, an intein (Cbu.DnaB) within dnaB and 29 insertion sequences.

8 or ammonia catabolism, iron acquisition, and insertion sequences.

9 polymorphisms, and a unique distribution of insertion sequences.

10 racketed by the homologous ISV-A1 and ISV-A2 insertion sequences.

11 st of which locate to intergenic regions and insertion sequences.

12 S1601 contains portions of three independent insertion sequences.

13 tive composite transposon bracketed by IS600 insertion sequences.

14 nucleotide changes, and the transposition of insertion sequences.

15 deletion via recombination between flanking insertion sequences.

16 harbors at least 12 copies of five distinct insertion sequences.

17 ation of the composite transposon's flanking insertion sequences.

18 ral mechanism for the formation of miniature insertion sequences.

19 n of all genomic rearrangements that involve insertion sequences.

20 re recognized: 13 capsule synthesis genes, 4 insertion sequences, 1 truncated biosynthesis gene, and

21 h several genomic rearrangements mediated by insertion sequences, 12 cryptic prophages, 372 pseudogen

22 time PCR assay with three targets, including insertion sequence 481 (IS481), IS1001, and an IS1001-li

23 in the United States, most laboratories use insertion sequence 481 (IS481), which is not specific fo

24 ary 1, 2001, and December 31, 2003, that had insertion sequence 6110 (IS6110) restriction fragment le

25 Insertion sequences, a phage genome, and/or loci from di

26 tative virulence genes, genomic islands, and insertion sequences across a collection of 33 strains is

27 While insertion sequence analysis using IS1634 clearly indicat

28 After removing rRNA, vector, bacterial insertion sequence and chimeric cDNA contaminants, small

29 ogenic bacterial plasmid "mobilome" includes insertion sequence and other transposable elements that

30 on is unusually G-C rich, and it has unusual insertion sequences and a minimal dependence on the EBS2

31 ing, sap typing, and the presence/absence of insertion sequences and a type I restriction modificatio

32 The genome is unusually rich in insertion sequences and displays anomalies in GC base-co

33 ither singly or in large multiple arrays, to insertion sequences and gene duplications of one kilobas

34 ools such as Optimized Annotation System for Insertion Sequences and IScan currently identify IS elem

35 plicated by the presence of repeat elements, insertion sequences and other similar factors that contr

36 strain chi7122 include complete and partial insertion sequences and phage-related DNA sequences, som

37 Divergent features included already reported insertion sequences and ragB, as well as additional hypo

38 n is a complex recombination event involving insertion sequences and repeat sequences.

39 omosome of each recipient, where it acquired insertion sequences and underwent deletions and rearrang

40 ransposon mutant library that is amenable to insertion sequencing and introduced this mutant pool int

41 olerae survival, and by combining transposon-insertion sequencing and transcriptomic data sets, we al

42 es-specific hypothetical genes, transposons, insertion sequences, and integrases and were located adj

43 wo strains exhibit differences in prophages, insertion sequences, and island structures.

44 d contains an unusual t-RNA island, numerous insertion sequences, and large repeated elements, includ

45 nactivated via frameshifts, point mutations, insertion sequences, and putative deletions.

46 ae are spread by plasmid-mediated integrons, insertion sequences, and transposons, some of which are

47 ke other obligate intracellular bacteria, 32 insertion sequences are found dispersed in the chromosom

48 Phages, phage-like elements, and insertion sequences are the major sources of variation b

49 mino acids of the peptide, also known as the insertion sequence, are found to be essential in reducin

50 While present in many bacterial insertion sequences as well as in the eukaryotic family

51 none of the C2 isolates) carried IS1016 (an insertion sequence associated with H influenzae capsule

52 Selenocysteine insertion sequence-associating factors, adenosine, and A

53 TA proteins possess a hydrophobic membrane insertion sequence at their C-terminus such that it can

54 Selenocysteine insertion sequence binding protein 2 (SBP2) is a critica

55 region of selenoprotein mRNAs as well as Sec insertion sequence binding protein 2, Sec-tRNA(Sec), and

56 by a multiprotein complex that includes Sec insertion sequence-binding protein 2 (SECISBP2; also kno

57 tetramer, where a USP25-specific, conserved insertion sequence blocks ubiquitin binding.

58 transposase, a member of the IS256 family of insertion sequences, bound to DNA substrates correspondi

59 rs to play a central role in the exchange of insertion sequences, but not the exchange of high-identi

60 ns of C. reinhardtii have short extension or insertion sequences, but overall the large subunit prote

61 ntify thousands of MGEs, including candidate insertion sequences, conjugative transposons, and propha

62 Recombination between insertion sequence copies can cause genetic deletion, in

63 present a resource and analysis of 2,363 new insertion sequences corresponding to 720 genomic loci.

64 We have refined analysis of transposon-insertion sequencing data by normalizing for the effect

65 iated information inherent in all transposon-insertion sequencing data sets.

66 The presence of an insertion sequence defines the major phylogenetic pre-se

67 ruption in the A genome include retroelement insertions, sequence deletions, and mutations causing in

68 Variant calling and insertion sequence detection were performed, focusing on

69 uence similarities to known genes, including insertion sequences, determinants of regulatory proteins

70 Insertion sequence disruption was limited to mgrB (P < .

71 /T rich (80%) and is an efficient target for insertion sequences during stationary phase.

72 eatures of the cDNA include a selenocysteine insertion sequence element approximately 4.8 kb 3' to th

73 on of mooV by the joining of the ends of the insertion sequence element at the circle junction.

74 Discrepancies between the insertion sequence element distribution patterns, the di

75 A common insertion sequence element in Escherichia coli, IS5, has

76 g from stop to Sec involves a cis-acting Sec insertion sequence element in the 3' untranslated region

77 ) and its insertion was dependent on the Sec insertion sequence element in the 3'UTR of TR1 mRNA.

78 rs713041 is located near the selenocysteine insertion sequence element in the GPX4 3' untranslated r

79 hia coli K-12 strain MG1655 contained an IS1 insertion sequence element in the regulatory region of t

80 The insertion sequence element is located on the plasmid bet

81 lis: (i) the transposition of the endogenous insertion sequence element IS1126 and (ii) the modulatio

82 determined that the endogenous P. gingivalis insertion sequence element IS1126 is capable of transpos

83 The insertion sequence element IS1358, found in both O1 and

84 A 155-159 bp insertion sequence element known as the Correia element,

85 depends on the nature of the selenocysteine insertion sequence element located in the 3' UTR of sele

86 the presence of a functional selenocysteine insertion sequence element that is highly active but onl

87 gly, however, we also observed that a 1.8-kb insertion sequence element was positioned between ccmB a

88 expressed when the Drosophila selenocysteine insertion sequence element was used, whereas the corresp

89 mRNA stem-loop structure, the selenocysteine insertion sequence element.

90 cal to that in O157:H7 is bounded by the IS1 insertion sequence element.

91 egion of the cDNA contains a canonical Secys insertion sequence element.

92 We describe the use of two insertion sequence elements (ISFtu1 and ISFtu2) in Franc

93 A total of 80 copies of three different insertion sequence elements are interspersed throughout

94 parent strain using all known P. gingivalis insertion sequence elements as probes suggested that no

95 idence that homologous recombination between insertion sequence elements can be a primary determinant

96 Among these are 85 predicted insertion sequence elements in eight different families.

97 The insertion sequence elements in the composite transposon-

98 conversion and several other loci containing insertion sequence elements or phage-related gene insert

99 gingivalis was a concerted up-regulation of insertion sequence elements related to IS1 transposases.

100 se genes, conjugative functions and multiple insertion sequence elements suggests that the PAI, or se

101 The genome contains numerous insertion sequence elements that have mediated extensive

102 Here, we performed RFLP analyses using Insertion Sequence elements to resolve the phylogenetic

103 em-loop structures resembling selenocysteine insertion sequence elements were identified in the 3'-un

104 Although many phage and insertion sequence elements were missing from the core c

105 frame is homologous to a family of putative insertion sequence elements, although our evidence shows

106 vel program that searches for selenocysteine insertion sequence elements, followed by selenoprotein g

107 PXO99A contains numerous copies of diverse insertion sequence elements, members of which are associ

108 accounted for by the presence or absence of insertion sequence elements.

109 vealed the presence of one or two classes of insertion sequence elements.

110 n to those previously known in dnaX and nine insertion sequence elements.

111 enome, characterized by a very high level of insertion sequences elements (ISs) and DNA repeats, for

112 Three "insertion" sequence elements present in POLQ are not fou

113 ariable deletion events between the flanking insertion-sequence elements, all resulting in eliminatio

114 including phage-derived genes, plasmids, and insertion-sequence elements, highlighting its dynamic na

115 o high-throughput DNA sequencing (transposon-insertion sequencing) enables simultaneous and genome-wi

116 analysis of BiXyn10A demonstrated that such insertion sequences encode a new family of carbohydrate-

117 g decay through loss of functional genes and insertion sequence expansion, often indicative of adapta

118 ar homologous recombination occurred between insertion sequences following an initial transposition e

119 Chimeric insertion sequence footprints were observed at the delet

120 cise, reading frame-restoring excision of an insertion sequence from the coding region of expR, a gen

121 action of biological meaning from transposon-insertion sequencing genomic data.

122 These insertion sequences have subsequently allowed the amplif

123 bile genetic elements such as transposons or insertion sequences, i.e. they possess direct repeats at

124 vPCR of insertion sequences identified these same mutations and

125 The locus is replaced by an insertion sequence in B. pertussis, explaining the lack

126 single event, the transposition of an IS6110 insertion sequence in one of the strains, accounted for

127 designated ISPpu12, had the structure of an insertion sequence in that it was bordered by 24-bp near

128 s, resulting in an overall high abundance of insertion sequences in the genomes.

129 ility of internal deletion variants of other insertion sequences in these isolates suggests that this

130 om multiple inversions of genome segments at insertion sequences, in a manner consistent with present

131 the sea urchin Tsp family and Drosophila SGM insertion sequences; in addition, they possess regions o

132 Recent studies revealed that a hydrophobic insertion sequence (INS) in these LAADs also interacts w

133 directed insertion site sequencing (TraDIS), insertion sequencing (INSeq) and high-throughput inserti

134 Here, we tested whether transposon insertion sequencing (INSeq) could be used to identify b

135 Insertion sequencing (INSeq) is a method for determining

136 ersed repetitive elements (SINEs), and of an insertion sequence (InsIpCHSD) found in the neighborhood

137 onal events involved the transposition of an insertion sequence into a narrow window of a single gene

138 Molecular fingerprinting with the IS6110 insertion sequence is useful for tracking transmission o

139 Transposon insertion sequencing is a high-throughput technique for

140 addition to homologs of two other H. pylori insertion sequence (IS) element genes, orfA, which encod

141 quence studied is derived from a Roseiflexus insertion sequence (IS) element where the resulting tran

142 Streptomyces scabies 84.34 identified a new insertion sequence (IS) element, IS1629, with homology t

143 up (SFG) R. peacockii, we identified a novel insertion sequence (IS) element, ISRpe1, disrupting the

144 ed many of the lines for mutations involving insertion sequence (IS) elements and identified two gene

145 her elements such as transposons, integrons, insertion sequence (IS) elements and the 'new' ISCR (IS

146 The insertion sequence (IS) elements are the smallest but mo

147 We found that insertion sequence (IS) elements are unusually abundant

148 Prokaryotic insertion sequence (IS) elements behave like parasites i

149 ly syntenous, recombination between abundant insertion sequence (IS) elements has resulted in genome

150 ns within functional cps loci, consisting of insertion sequence (IS) elements in unique positions tha

151 he 16 kb region in P. furiosus is flanked by insertion sequence (IS) elements with inverted and direc

152 espite its small size, the genome harbors 73 insertion sequence (IS) elements, almost all of which ar

153 ltiple members of two classes of Francisella insertion sequence (IS) elements, ISFtu1 and ISFtu2, and

154 e plasmid harbors a 16-kb region, flanked by insertion sequence (IS) elements, that encodes the restr

155 , we present genetic maps of recently active Insertion Sequence (IS) elements, the simplest form of M

156 nes, a possible new replicon, and two intact insertion sequence (IS) elements.

157 ents involve mobile genetic elements such as insertion sequence (IS) elements.

158 y to the transposition of direct repeats and insertion sequence (IS) elements.

159 of these were related to known and putative insertion sequence (IS) elements; no known bacterial pla

160 An insertion sequence (IS) excision enhancer (IEE) was disc

161 Here, we describe the first insertion sequence (IS) identified from R. salmoninarum.

162 1998, for which the W family was defined by insertion sequence (IS) IS6110 DNA fingerprinting, polym

163 A new insertion sequence (IS) of Mycoplasma fermentans is desc

164 a highly diagnostic set of markers based on insertion sequence (IS) site polymorphism and genomic re

165 G1655, resulting from a dramatic increase in insertion sequence (IS) transposition, especially IS150.

166 ssibility, we have studied the occurrence of insertion sequence (IS)-like elements in P. gingivalis W

167 d hurdle, DNA-protein crosslinking (DPC), by insertion sequence (IS)-mediated copy number variations

168 ycobacterium tuberculosis isolates underwent insertion sequence (IS)6110 restriction-fragment-length

169 Complete and fragmented insertion sequences (IS) make up 24% of the total DNA an

170 Nearly 40% of the prophages harbored insertion sequences (IS) previously described in H. pylo

171 a harbor simple transposable elements termed insertion sequences (IS).

172 P4 prophage-like integrase gene and numerous insertion sequences (IS).

173 ent length polymorphism (RFLP) analysis with insertion sequences IS100 and IS285 as probes.

174 An additional molecular marker, insertion sequence IS1301, was found to be present in 10

175 he isolates resulted from the presence of an insertion sequence, IS1301, in the intergenic region (IG

176 the ser2 gene cluster are flanked by a novel insertion sequence (IS1601) oriented as direct repeats.

177 three of these isolates, a newly discovered insertion sequence, IS1630 (of the IS30 class), was loca

178 PCR assays targeting insertion sequence IS481 (IS), pertussis toxin ptxA prom

179 se-developed PCR test targeting the repeated insertion sequence IS481 for the detection of Bordetella

180 The insertion sequence IS481 is also present in Bordetella h

181 This assay (LC-PCR-IS) targets the insertion sequences IS481 and IS1001 of B. pertussis and

182 o those of a nested-PCR method targeting the insertion sequences IS481 and IS1001.

183 The mycobacterial insertion sequence IS6110 has been exploited extensively

184 insertion of the Mycobacterium tuberculosis insertion sequence IS6110.

185 The Mycobacterium tuberculosis-specific insertion sequence IS6110/986 has been widely used as a

186 The genome of M. tuberculosis carries insertion sequences (IS6110) that are relatively stable

187 The mobile insertion sequence, IS6110, is an important marker in tr

188 The bacterial insertion sequence IS903 has the unusual ability to tran

189 Like many transposons the bacterial insertion sequence IS903 was thought to insert randomly.

190 additional copy of the previously identified insertion sequence ISMi1 was cloned.

191 A 3,372-bp insertion sequence, ISPpu12, has been identified on the

192 tial mobile units (PMUs), which contain tra5 insertion sequences (ISs) and genes for specialized sigm

193 Analyses of complete genomes indicate that insertion sequences (ISs) are abundant and widespread in

194 Insertion sequences (ISs) are simple transposable elemen

195 Insertion sequences (ISs) are transposable elements pres

196 COM1 also has 45 full or partial insertion sequences (ISs) compared to 35 in the referenc

197 Bacterial insertion sequences (ISs) from the IS200/IS605 family en

198 nd B. holmesii was developed using multicopy insertion sequences (ISs) in combination with the pertus

199 Like the three other insertion sequences (ISs) known in this gastric pathogen

200 hat are part of transposable elements called insertion sequences (ISs).

201 ular forms are also known for some bacterial insertion sequences (ISs).

202 A-2-3B'a(2-13) each host several families of insertion sequences (ISSoc families) at various copy num

203 Both tet(X3) and tet(X4) are adjacent to insertion sequence ISVsa3 on their respective conjugativ

204 The Synechocystis sp. PCC6803 insertion sequence ISY100 (ISTcSa) belongs to the Tc1/ma

205 Tandem amplification occurs via the flanking insertion sequences, leading to increased toxin producti

206 The insertion sequence led to an increase in the transcript

207 anatomical images, transgenic constructs and insertions, sequence-level gene models and molecular cla

208 ites that occurred within the selenocysteine insertion sequence-like structures.

209 asses: (i) proviruses, (ii) casposons, (iii) insertion sequence-like transposons, (iv) integrative-co

210 This region also contains IS492, an insertion sequence located numerous times throughout a r

211 Extensive insertion sequence-mediated genome rearrangements and re

212 r bacterial NusG proteins contain a variable insertion sequence of approximately 70 residues in the c

213 performed DNA fingerprinting with the IS6110 insertion sequence of the organisms isolated from patien

214 this hypothesis, a mutation in the membrane insertion sequence of the v-SNARE synaptobrevin/vesicle-

215 sition cycle, has recently been proposed for insertion sequences of the IS3 family.

216 cur through homologous recombination between insertion sequences on both sides of a duplicated region

217 i are bracketed by or are in the vicinity of insertion sequences or long clusters of tandem repeats (

218 inding could be explained by the presence of insertion sequences or mutations in O-antigen or lipopol

219 me is unusual in that there are virtually no insertion sequences or phage-associated sequences and ve

220 oxin, mycolactone, as well as by hundreds of insertion sequences, particularly IS2404.

221 IS1381, an insertion sequence previously described in Streptococcus

222 e sequence in the rDNA, with the most common insertion sequences promoting faster processing.

223 dons with the help of a putative pyrrolysine insertion sequence (PYLIS) element.

224 lation, but loss of a downstream pyrrolysine insertion sequence (PYLIS) significantly increased the U

225 a dynamic 2,571,010-bp genome containing 91 insertion sequences representing 12 families and organiz

226 archy of selenoprotein synthesis are the Sec insertion sequence RNA-binding proteins, SBP2 and nucleo

227 taining N-terminal extensions (S2 and S5) or insertion sequence (S3).

228 cess are the mRNA binding protein of the Sec insertion sequence, SBP2, and the specialized elongation

229 In a transposon-insertion sequencing screen to identify mutants syntheti

230 a 3 untranslated region (UTR) selenocysteine insertion sequence (SECIS) and the SECIS-binding protein

231 ing event is specified by the selenocysteine insertion sequence (SECIS) element and requires the sele

232 It is thought that the SelenoCysteine Insertion Sequence (SECIS) element and UGA codon are suf

233 c in mammalian selenoproteins requires a Sec insertion sequence (SECIS) element in the 3' untranslate

234 codon as selenocysteine (Sec) requires a Sec insertion sequence (SECIS) element in the 3' untranslate

235 re a set of highly specific factors: the Sec insertion sequence (SECIS) element in the 3' untranslate

236 rporation into selenoproteins requires a Sec Insertion Sequence (SECIS) element in the 3' untranslate

237 A selenocysteine insertion sequence (SECIS) element in the 3'-untranslate

238 ec-dedicated elongation factor SelB to a Sec insertion sequence (SECIS) element in the selenoprotein-

239 ated at UGA codons in mRNAs possessing a Sec insertion sequence (SECIS) element in their 3'-untransla

240 egion of this gene contains a selenocysteine insertion sequence (SECIS) element that deviates at one

241 two copies of tRNA-Sec and a selenocysteine insertion sequence (SECIS) element which were lost in pl

242 of UGA as Sec depends on the selenocysteine insertion sequence (SECIS) element, a stem-loop structur

243 aryotes, incorporation of Sec requires a Sec insertion sequence (SECIS) element, a stem-loop structur

244 a common stem-loop structure, selenocysteine insertion sequence (SECIS) element, that is necessary fo

245 The Sec insertion sequence (SECIS) element, which is the stem-lo

246 ependent on the presence of a selenocysteine insertion sequence (SECIS) element, which recruits the s

247 stream of a stem-loop structure known as Sec insertion sequence (SECIS) element.

248 ns as selenocysteine is specified by the Sec insertion sequence (SECIS) element.

249 acting mRNA structure, called selenocysteine insertion sequence (SECIS) element.

250 ons requires a cis-acting RNA structure, Sec insertion sequence (SECIS) element.

251 odon UGA with the help of the selenocysteine insertion sequence (SECIS) element.

252 the presence of a cis-acting selenocysteine insertion sequence (SECIS) element.

253 ranslated region (UTR), referred to as a Sec insertion sequence (SECIS) element.

254 ppresses UGA codons that are upstream of Sec insertion sequence (SECIS) elements bound by SECIS-bindi

255 ly structured 3' UTR contains selenocysteine insertion sequence (SECIS) elements that are required fo

256 selenoprotein genes contained selenocysteine insertion sequence (SECIS) elements that were similar, b

257 y identified several genes with multiple Sec insertion sequence (SECIS) elements, one of which was a

258 for evolutionarily conserved selenocysteine insertion sequence (SECIS) elements, which are RNA struc

259 to UGA codons is directed by selenocysteine insertion sequence (SECIS) elements.

260 n selenoproteins depends on a selenocysteine insertion sequence (SECIS) in the 3'-UTR of mRNAs of euk

261 gency of the Escherichia coli selenocysteine insertion sequence (SECIS) requirements, libraries of SE

262 sertion requires a cis-acting selenocysteine insertion sequence (SECIS) usually located in the 3'UTR

263 untranslated region, termed a selenocysteine insertion sequence (SECIS), and SECIS-binding protein 2

264 ires the TGA opal codon and a downstream Sec insertion sequence (SECIS), which can be partially rando

265 ecific mRNA sequence known as selenocysteine insertion sequence (SECIS).

266 tructure and stability of the selenocysteine insertion sequences (SECIS) of human glutathione peroxid

267 g genomic deletions of 3' UTR selenocysteine-insertion-sequences (SECIS1 and SECIS2).

268 e subspecies and is bracketed by remnants of insertion sequences, suggesting a multistep process in t

269 Here, a transposon insertion sequencing technology called INSeq was used to

270 repeat (NR) and 3' NR] of the gene and in an insertion sequence that precedes the 3' NR region.

271 kynyliodonium salt/alkylidenecarbene/1,5 C-H insertion sequence that sets the pivotal quaternary cent

272 Downstream from the termination codon is an insertion sequence that was homologous to the ISVs1 elem

273 We discover 525 new insertion sequences that are not present in the human re

274 pproximately 5% of the genome is composed of insertion sequences that may contribute to genome rearra

275 ntify the chromosomal position of repetitive insertion sequences that typically flank horizontally ac

276 xpression levels of endogenous and exogenous insertion sequences that were 2 orders of magnitude high

277 uctural features, pathognomonic of a regular insertion sequence, this element was designated IS1414.

278 since the introduction of modern transposon-insertion sequencing (TIS) methods, which combine genome

279 ed mutagenesis in a method termed transposon insertion sequencing (TIS).

280 e-gene deletion strains and a new transposon insertion sequencing (Tn-Seq) dataset that we generated.

281 Transposon insertion sequencing (Tn-Seq) is a microbial systems-lev

282 Transposon insertion sequencing (Tn-seq) is an emerging technology

283 We used transposon insertion sequencing (Tn-Seq) to define essential genes

284 Here we use transposon insertion sequencing to identify A. baumannii mutants di

285 We applied high-throughput insertion sequencing to identify which bacterial genes a

286 We used transposon-insertion sequencing to screen for genes that contribute

287 racterized by means of a Transposon Directed Insertion Sequencing (TraDIS) approach.

288 previously developed the Transposon Directed Insertion Sequencing (TraDIS) protocol for this purpose,

289 n IR resistance by using transposon-directed insertion sequencing (TraDIS).

290 e analysis revealed the presence of multiple insertion sequences upstream and downstream of the aerob

291 ion studies of Acinetobacter baylyi ADP1, an insertion sequence was evident in approximately 2% of th

292 genomic DNA and, except for one deletion, an insertion sequence was found at the break point.

293 steria monocytogenes, although the consensus insertion sequence was the same.

294 a-D-glucosidase gene, with a novel PA14-like insertion sequence, was identified two genes downstream

295 As in the absence of thiI Through transposon insertion sequencing, we identified additional tRNA modi

296 Most insertion sequences were derived from homologous positio

297 Forty-eight unique insertion sequences were detected in the first animal an

298 ed OASIS, or Optimized Annotation System for Insertion Sequences, which automatically annotates ISs w

299 in is distinctive in its large complement of insertion sequences, with several genomic rearrangements

300 ces, a Y chromosome-specific sequence, or an insertion sequence within the glutathione S-transferase