ライフサイエンスコーパス: polytene chromosome

1 ion, resulting in underreplicated domains of polytene chromosomes.

2 in the formation of a single chromocenter in polytene chromosomes.

3 ed its distribution on larval salivary gland polytene chromosomes.

4 CAF-1 p105 colocalized in vivo in Drosophila polytene chromosomes.

5 to the heterochromatic regions of Drosophila polytene chromosomes.

6 (activated 20E-regulated genes) forms on the polytene chromosomes.

7 transcriptionally active sites on Drosophila polytene chromosomes.

8 map of An. funestus using ovarian nurse cell polytene chromosomes.

9 ploid interphase and mitotic chromosomes and polytene chromosomes.

10 both affected the binding pattern of E(z) on polytene chromosomes.

11 aracterized their localization on Drosophila polytene chromosomes.

12 SIN3 and RPD3 to DROSOPHILA: salivary gland polytene chromosomes.

13 in vitro and colocalize at specific sites on polytene chromosomes.

14 located at >200 distinct sites on Drosophila polytene chromosomes.

15 ingle-copy gene that maps to position 49B on polytene chromosomes.

16 ng region and it maps to position 94B1-B2 on polytene chromosomes.

17 east two introns and maps to position 21D on polytene chromosomes.

18 enetic histories, especially in insects with polytene chromosomes.

19 le copy gene and maps to position 86D5-10 on polytene chromosomes.

20 se II (pol II) at developmental puffs on the polytene chromosomes.

21 proteins that associate with normal sites in polytene chromosomes.

22 nit of NURF and is generally associated with polytene chromosomes.

23 d at numerous sites along the salivary gland polytene chromosomes.

24 ic regions along the euchromatic arms of the polytene chromosomes.

25 le copy gene and maps to position 92F-93A on polytene chromosomes.

26 mes, as well as at > 400 euchromatic loci on polytene chromosomes.

27 D1 homologue (dCHD1) and its localization on polytene chromosomes.

28 d fixed paracentric inversions detectable in polytene chromosomes.

29 r class of mutation affected NONA binding to polytene chromosomes.

30 third chromosome by in situ hybridization to polytene chromosomes.

31 iately upstream of para in region 14D of the polytene chromosomes.

32 n (BiFC) analysis of protein interactions on polytene chromosomes.

33 ocalizing with RNA polymerase II (Pol II) on polytene chromosomes.

34 C subunits colocalize in euchromatic arms of polytene chromosomes.

35 increase the stability of cohesin binding to polytene chromosomes.

36 ongating RNA polymerase II on salivary gland polytene chromosomes.

37 veral transcriptionally active interbands of polytene chromosomes.

38 visualization of altered O-GlcNAc cycling on polytene chromosomes.

39 sociate with hundreds of sites on Drosophila polytene chromosomes.

40 e boundaries between bands and interbands in polytene chromosomes.

41 1 also localizes to most transcribed loci on polytene chromosomes.

42 ed its distribution on larval salivary gland polytene chromosomes.

43 ning but also intronless genes on Drosophila polytene chromosomes.

44 g4)2.2 and colocalizes with both proteins on polytene chromosomes.

45 cally increased in both ash2 and sktl mutant polytene chromosomes.

46 rated at transcriptionally active regions on polytene chromosomes.

47 uorescence staining of larval salivary-gland polytene chromosomes.

48 d H4 and H3 in both transgenes in Drosophila polytene chromosomes.

49 ected at transcriptionally active regions of polytene chromosomes.

50 ively transcribed Pol II genes on Drosophila polytene chromosomes.

51 nd produce four-stranded diplochromosomes or polytene chromosomes.

52 somes without separation frequently produces polytene chromosomes, a barrier to accurate mitosis.

53 and E(Z) colocalize virtually completely on polytene chromosomes and are associated with a subset of

54 teins colocalize on several hundred sites on polytene chromosomes and are distributed in a punctated

55 ranscriptionally active chromosomal sites on polytene chromosomes and are rapidly recruited to endoge

56 Bon is associated with sites on the polytene chromosomes and can interact with numerous Dros

57 supported by immunofluorescence staining of polytene chromosomes and cell lines, and these studies a

58 SIR2 binds to many euchromatic sites on polytene chromosomes and colocalizes with E(Z) at most s

59 tionally active puff sites within Drosophila polytene chromosomes and exhibits many of the expected b

60 cDNA clones enabled us to map the genes on polytene chromosomes and identify for the first time the

61 ifically to euchromatic interband regions of polytene chromosomes and is enriched 2-fold on the male

62 localizes extensively with DOM on Drosophila polytene chromosomes and is recruited to sites of active

63 to the gene-rich interband regions of larval polytene chromosomes and is upregulated almost 2-fold on

64 Combining in situ hybridization to polytene chromosomes and long-range PCR, we have identif

65 Elba2 protein is distributed ubiquitously in polytene chromosomes and strongly colocalizes with H1.

66 rrelation between the number of bands on the polytene chromosomes and the 20 genes identified by conv

67 R-Ultraspiracle (USP) heterodimer to bind to polytene chromosomes and the promoters of EcR target gen

68 D3, RBF1 and dCAP-D3 partially colocalize on polytene chromosomes, and RBF1 is required for efficient

69 lso colocalize extensively on salivary gland polytene chromosomes, and reducing Nipped-A activity dec

70 n effect variegation, molds the structure of polytene chromosomes, and should be investigated for pos

71 of steroid-regulated and cell death genes on polytene chromosomes, and the expression of these genes

72 ands and the heterochromatic chromocenter of polytene chromosomes, and the H2Av antibody precipitated

73 In JIL-1 hypomorphs, euchromatic regions of polytene chromosomes are severely reduced and the chromo

74 mes are improperly condensed in mutants, and polytene chromosomes are structurally abnormal and disor

75 e recruited to unique and shared sites along polytene chromosome arms.

76 lta is present at the chromocenter on larval polytene chromosomes as well as at discrete bands inters

77 ther necessary nor sufficient for the stable polytene chromosome association of SU(S).

78 Pc, Psc, Scm, E(z) and Ph remain bound to polytene chromosomes at most sites in the absence of Pho

79 k gene family, Hsp70 (Hsp70Aa and Hsp70Ab in polytene chromosome band 87A, and Hsp70Bb in 87C).

80 leoplasm and in association with a subset of polytene chromosome bands.

81 Ectopic expression of DHR3 revealed that the polytene chromosome binding pattern is of functional sig

82 of Drosophila melanogaster, was localized in polytene chromosomes by indirect immunofluorescence and

83 Second, reduplicated polytene chromosomes can also separate prior to metaphas

84 ced using cytogenetic mapping to mitotic and polytene chromosomes, clone-based finishing and BAC fing

85 ociate with specific sites on salivary gland polytene chromosomes, colocalizing with many Trx binding

86 Analyses using immunolocalization on polytene chromosomes confirm the involvement of these do

87 63F early puff in the larval salivary gland polytene chromosomes contains the divergently transcribe

88 Immunofluorescence analysis of polytene chromosomes corroborated the cross-linking resu

89 ne is sufficient to rescue JIL-1 null mutant polytene chromosome defects including those of the male

90 In situ hybridization to salivary gland polytene chromosomes determined that both ends of each i

91 The complex banding pattern of H2Av in polytene chromosomes did not parallel the concentration

92 Importantly, TRF2-depleted polytene chromosomes display severe chromosomal structur

93 hat the acetylation of histones H3 and H4 in polytene chromosomes does not change during heat shock.

94 t Wapl-dependent release from salivary gland polytene chromosomes during interphase and from neurobla

95 th dSpt6 at transcriptionally active loci on polytene chromosomes during normal development and are s

96 ith elongating RNA polymerase II (Pol II) on polytene chromosomes, elongating Pol II can persist on c

97 Polytene chromosomes exhibit intricate higher order chro

98 The map positions on polytene chromosomes for dHDAC1 and dHDAC3 were determin

99 -2 transcripts accumulate after the onset of polytene chromosome formation and remain high throughout

100 HP1 immunostaining on polytene chromosomes from Drosophila larval salivary gla

101 rs SPT6 and CHD1 are dramatically reduced on polytene chromosomes from kis mutant larvae.

102 ned the distribution of five PcG proteins on polytene chromosomes from pho-like, pho double mutants.

103 ith high transcriptional activity (puffs) on polytene chromosomes from salivary glands of third insta

104 any late S phase; during these cycles a new polytene chromosome grows from each 2C chromatid pair to

105 The exceptional cytology provided by polytene chromosomes has made Drosophila melanogaster a

106 The cytogenetic locations on the nurse cell polytene chromosomes have been determined for 47 markers

107 rly 1960s, imaging studies of Drosophila sp. polytene chromosomes have provided unique views of gene

108 osomal loci in euchromatin of salivary gland polytene chromosomes, however, it also displays a strong

109 On Drosophila polytene chromosomes HP1 is localized to centric regions

110 On Drosophila polytene chromosomes, HP1 localizes to centric and telom

111 In polytene chromosomes, HP2 and HP1 colocalize at the chro

112 Several in vivo approaches, including polytene chromosome immunofluorescence, nuclear run-on a

113 R assays of chromatin immunoprecipitates and polytene chromosome immunofluorescence.

114 Using polytene chromosome immunostaining of other species from

115 Genetic mapping, Southern blotting, polytene chromosome in situ hybridization and DNA sequen

116 TS) content, restriction fingerprinting, and polytene chromosome in situ hybridization approaches wer

117 x and engrailed PREs, and that Spps binds to polytene chromosomes in a pattern virtually identical to

118 of open chromatin domains include 'puffs' on polytene chromosomes in Drosophila and extended loops fr

119 HP1 from the heterochromatic chromocenter of polytene chromosomes in larval salivary glands.

120 owever, these mutant proteins do bind to the polytene chromosomes in nurse-cell nuclei and enter the

121 oliferating cells, but not disaggregation of polytene chromosomes in salivary glands.

122 us are precisely excised during formation of polytene chromosomes in the developing macronucleus.

123 red for the association of SU(S) with larval polytene chromosomes in vivo.

124 bound to many ecdysone-induced puffs in the polytene chromosomes, including the early puffs that enc

125 BEAF binds to hundreds of sites on polytene chromosomes, indicating that BEAF-utilizing ins

126 ontrol of the puffing sequence on Drosophila polytene chromosomes initiated by the molting hormone 20

127 The JIL-1 kinase localizes to Drosophila polytene chromosome interbands and phosphorylates histon

128 r organization of pericentric regions of all polytene chromosomes into a single chromocenter.

129 In situ hybridization to Drosophila polytene chromosomes is a powerful tool for determining

130 distribution of dCDK12 on formaldehyde-fixed polytene chromosomes is virtually identical to that of h

131 uding the portion that appears banded in the polytene chromosomes, is heterochromatic; the banded reg

132 the gene encoding this cDNA to region A2b on polytene chromosome IV, the locus of the special lobe-sp

133 ar the borders of a structural domain in the polytene chromosomes, known as a puff, produced by trans

134 Mad2 delays anaphase separation of metaphase polytene chromosomes, Mad2's control of overall mitotic

135 crosatellites have been physically mapped to polytene chromosomes, making it possible to select loci

136 In Drosophila, the availability of polytene chromosome maps and of sets of probes covering

137 The first photographic polytene chromosome maps for D. montana and D. novamexic

138 Each section reviews the history of the polytene chromosome maps for each species, presents the

139 some maps for each species, presents the new polytene chromosome maps, and anchors the genomic scaffo

140 he level of light microscopic examination of polytene chromosomes, may not always be monophyletic.

141 In Drosophila S2 cells, and on polytene chromosomes, methyl-Lys 27 and Pc are both excl

142 autosome as well as partially rescue male X polytene chromosome morphology.

143 Lack of BEAF causes a disruption of male X polytene chromosome morphology.

144 of a telomeric DNA sequence isolated from a polytene chromosome of a hypotrichous ciliate folds back

145 correspond with the bands and interbands of polytene chromosomes of Drosophila.

146 The ASH1 protein is localized on polytene chromosomes of larval salivary glands at > 100

147 wever, DNA puffs of the salivary gland giant polytene chromosomes of Sciara coprophila undergo DNA am

148 Heat shock loci in the polytene chromosomes of the fruit fly Drosophila undergo

149 tion of 20 markers on the genetic map to the polytene chromosomes of the Hessian fly indicated good c

150 induces a small number of early puffs in the polytene chromosomes of the larval salivary gland.

151 . funestus complementary DNAs (cDNAs) to the polytene chromosomes of this species.

152 s can remain attached and aligned, producing polytene chromosomes, or they can be dispersed (Figure 1

153 re viability without rescuing the defects in polytene chromosome organization.

154 tin-associated protein whose distribution in polytene chromosomes overlaps with HP1a and appears to b

155 First, when reduplicated polytene chromosomes persist into metaphase, an anaphase

156 genes in a primary response made visible by polytene chromosome puffs.

157 sed based on observations of the activity of polytene chromosome "puffs" which distinguished "early"

158 n the 640-kb region of the third chromosome (polytene chromosome region 76B-D) that includes Chd3.

159 Immunohistochemical detection of Mam on polytene chromosomes revealed binding at > 100 sites.

160 Scm-SAM domain in long contiguous regions on polytene chromosomes revealed its independent ability to

161 u hybridization of lambda 20p1.4 to isolated polytene chromosomes revealed localization at the chromo

162 Antibody staining of embryos and polytene chromosomes reveals cell type-specific expressi

163 Studies of H1-depleted salivary gland polytene chromosomes show that H1 participates in severa

164 bution of SNR1 and BRM on the salivary gland polytene chromosomes showed that the Brm complex associa

165 Immunofluorescence analysis of polytene chromosomes shows extensive colocalization of t

166 The S6k gene, located at polytene chromosome site 65D, gives rise to two predomin

167 RF and these two proteins colocalize at many polytene chromosome sites containing RNA pol III genes.

168 colocalization of the Scm and ph proteins at polytene chromosome sites in vivo.

169 rylation antibodies, as well as an acid-free polytene chromosome squash protocol that preserves the a

170 Polytene chromosome staining, chromatin immunoprecipitat

171 Polytene chromosome structure is a characteristic of som

172 ense during late S phase and that nurse cell polytene chromosome structure is controlled by regulatin

173 nd display reduced cell division and altered polytene chromosome structure.

174 viability and the establishment of a normal polytene chromosome structure.

175 colocalize with RNA Pol II on salivary gland polytene chromosomes, suggesting a possible role for ISW

176 SU(VAR)2-10 is present at some polytene chromosome telomeres, and FISH analyses in muta

177 In transcriptionally active polytene chromosomes, the male and female proteins bind

178 D at actively transcribed loci on Drosophila polytene chromosomes under both normal and heat shocked

179 ear and spatial organization of An. funestus polytene chromosomes was compared with the best-studied

180 Myb accumulation and binding to polytene chromosomes was dependent on the core factors o

181 Combined with the effects on male X polytene chromosomes, we conclude that BEAF function aff

182 direct measurements on light micrographs of polytene chromosomes, we then deduce the states of chrom

183 apan, macrogenomic profiles derived from its polytene chromosomes were compared with those of mainlan

184 -specific differential composition of MMB in polytene chromosomes where some loci were bound by a Myb

185 ADs correspond to decompacted inter-bands of polytene chromosomes, whereas TADs mostly correspond to

186 localizes to the interbands and puffs of the polytene chromosomes, which are classic sites of transcr

187 I (TopI) to sites of localized DNA damage in polytene chromosomes within live cells of optically thic

188 dNlp from previously transcribed regions of polytene chromosome without redistribution to the heat s