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Links from GEO DataSets

Items: 20

1.

Non-canonical compensation of zygotic X transcription in Drosophila melanogaster development revealed through single embryo RNA-Seq

(Submitter supplied) We sequenced mRNA from 24 single D. melanogaster embryos (12 male and 12 female) taken from 8 early embryonic timepoints to generate the first sex specific timecourse of gene expression in early Drosophila development
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9061
24 Samples
Download data: BEDGRAPH, CUFF, SAM
Series
Accession:
GSE25180
ID:
200025180
2.

Zelda binding in the early Drosophila melanogaster embryo marks regions subsequently activated at the maternal-to-zygotic transition

(Submitter supplied) The earliest stages of development in most metazoans are driven by maternally deposited proteins and mRNAs, with widespread transcriptional activation of the zygotic genome occurring hours after fertilization, at a period known as the maternal-to-zygotic transition (MZT). In Drosophila, the MZT is preceded by the transcription of a small number of genes that initiate sex determination, patterning and other essential developmental processes. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11203
3 Samples
Download data: BED, BEDGRAPH
Series
Accession:
GSE30757
ID:
200030757
3.

Sex bias and maternal contribution to gene expression divergence in Drosophila blastoderm embryos

(Submitter supplied) Early embryogenesis is a unique developmental stage where genetic control of development is handed off from mother to zygote. Yet the contribution of this transition to the evolution of gene expression is poorly understood. Here we study two aspects of gene expression specific to early embryogenesis in Drosophila: sex-biased gene expression prior to the onset of canonical X chromosomal dosage compensation, and the contribution of maternally supplied mRNAs. more...
Organism:
Drosophila melanogaster; Drosophila pseudoobscura; Drosophila yakuba; Drosophila virilis
Type:
Expression profiling by high throughput sequencing
4 related Platforms
31 Samples
Download data: TXT
Series
Accession:
GSE68062
ID:
200068062
4.

The zinc finger protein Zelda plays a key role in the maternal to zygotic transition in Drosophila

(Submitter supplied) In all animals, the initial events of embryogenesis are controlled by maternal gene products that are deposited into the developing oocyte. At some point after fertilization, control of embryogenesis is transferred to the zygotic genome in a process called the maternal to zygotic transition (MZT). During this time maternal RNAs are degraded and zygotic RNAs are transcribed1. A long standing question has been, what factors regulate these events? The recent findings that microRNAs and Smaugs mediate maternal transcript degradation brought new life to this old problem2,3, however, the transcription factors that activate zygotic gene expression remained elusive. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by array
Dataset:
GDS3477
Platform:
GPL1322
6 Samples
Download data: CEL
Series
Accession:
GSE11231
ID:
200011231
5.
Full record GDS3477

Zinc finger protein Zelda deficiency effect on the embryo

Analysis of embryos lacking the zinc finger protein Zelda. Results provide insight into the role of Zelda in the transfer of control of embryogenesis to the zygotic genome during the process of maternal-to-zygotic transition.
Organism:
Drosophila melanogaster
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL1322
Series:
GSE11231
6 Samples
Download data: CEL
6.

X chromosome dosage compensation via enhanced transcriptional elongation in Drosophila males (Control & MSL2 RNAi)

(Submitter supplied) MSL (Male-specific lethal) complex increases transcription on the single X chromosome of Drosophila males in order to equalize expression of X-linked genes between males (XY) and females (XX). The increase in transcript levels correlates with MSL- dependent acetylation of histone H4 at K16 within the bodies of active genes, but identification of the transcriptional step affected has not been possible. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9061
12 Samples
Download data: TXT
Series
Accession:
GSE25887
ID:
200025887
7.

X chromosome dosage compensation via enhanced transcriptional elongation in Drosophila males (Untreated)

(Submitter supplied) MSL (Male-specific lethal) complex increases transcription on the single X chromosome of Drosophila males in order to equalize expression of X-linked genes between males (XY) and females (XX). The increase in transcript levels correlates with MSL- dependent acetylation of histone H4 at K16 within the bodies of active genes, but identification of the transcriptional step affected has not been possible. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9061
3 Samples
Download data: TXT
Series
Accession:
GSE25321
ID:
200025321
8.

Progressive dosage compensation during Drosophila embryogenesis is reflected by gene arrangement on the X chromosome

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL19951
96 Samples
Download data: BEDGRAPH, TAB
Series
Accession:
GSE127177
ID:
200127177
9.

Progressive dosage compensation during Drosophila embryogenesis is reflected by gene arrangement on the X chromosome [RNA-seq]

(Submitter supplied) In D. melanogaster males, X chromosome monosomy is compensated by chromosome-wide transcription activation. We found that complete dosage compensation during embryogenesis takes surprisingly long. Although the activating Dosage Compensation Complex (DCC) associates with the chromosome and acetylates histone H4 early, many genes are not compensated. Acetylation levels on gene bodies continue to increase for several hours after gastrulation in parallel with progressive compensation. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19951
54 Samples
Download data: TAB
Series
Accession:
GSE127176
ID:
200127176
10.

Progressive dosage compensation during Drosophila embryogenesis is reflected by gene arrangement on the X chromosome [ChIP-seq]

(Submitter supplied) In D. melanogaster males, X chromosome monosomy is compensated by chromosome-wide transcription activation. We found that complete dosage compensation during embryogenesis takes surprisingly long. Although the activating Dosage Compensation Complex (DCC) associates with the chromosome and acetylates histone H4 early, many genes are not compensated. Acetylation levels on gene bodies continue to increase for several hours after gastrulation in parallel with progressive compensation. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19951
42 Samples
Download data: BED, BEDGRAPH
Series
Accession:
GSE127175
ID:
200127175
11.

Sex-specific embryonic gene expression in species with newly evolved sex chromosomes

(Submitter supplied) Sex chromosome dosage differences between males and females are a significant form of natural genetic variation in many species. Like many species with chromosomal sex determination, Drosophila females have two X chromosomes, while males have one X and one Y. The model species D. melanogaster has five roughly equally sized chromosome arms, one of which is the X chromosome. However, fusions of sex chromosomes with autosomes have occurred along the lineage leading to D. more...
Organism:
Drosophila miranda; Drosophila pseudoobscura
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18087 GPL13310
96 Samples
Download data: TXT
Series
Accession:
GSE53483
ID:
200053483
12.

Evolution of maternal and zygotic mRNA complements in the early Drosophila embryo

(Submitter supplied) The earliest stage of animal development is controlled by maternally deposited mRNA transcripts and proteins. Once the zygote is able to transcribe its own genome, maternal transcripts are degraded, in a tightly regulated process known as the maternal to zygotic transition (MZT). While this process has been well-studied within model species, we have little knowledge of how the pools of maternal and zygotic transcripts evolve. more...
Organism:
Drosophila melanogaster; Drosophila yakuba; Drosophila ananassae; Drosophila erecta; Drosophila miranda; Drosophila sechellia; Drosophila simulans; Drosophila virilis; Drosophila mauritiana; Drosophila mojavensis; Drosophila pseudoobscura; Drosophila willistoni; Drosophila persimilis; Drosophila santomea
Type:
Expression profiling by high throughput sequencing; Third-party reanalysis
14 related Platforms
119 Samples
Download data: TXT
Series
Accession:
GSE112858
ID:
200112858
13.

Small RNAs from third instar Drosophila melanogaster males

(Submitter supplied) The goal of this study was to determine if small RNAs from the 1.688 g/cm 3 satellite repeats are present in male larvae.
Organism:
Drosophila melanogaster
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL13304
4 Samples
Download data: TXT
Series
Accession:
GSE61846
ID:
200061846
14.

Differential Chromatin Binding of the Drosophila Dosage Compensation Complex

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by genome tiling array; Genome binding/occupancy profiling by high throughput sequencing
4 related Platforms
27 Samples
Download data: PAIR
Series
Accession:
GSE37865
ID:
200037865
15.

ChIP-Seq profiles of MSL1, MSL2, MSl3, MOF, MLE, H4K16ac and RNA Polymerase II phosphorlyated on Serine 5 in Drosophila S2 cells

(Submitter supplied) ChIP-Seq profiles of MSL1, MSL2, MSl3, MOF, MLE, H4K16ac and RNA Polymerase II phosphorlyated on Serine 5 in Drosophila S2 cells
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13304 GPL9058 GPL9061
17 Samples
Download data: BEDGRAPH
Series
Accession:
GSE37864
ID:
200037864
16.

ChIP-chip profiles of MLE, MSL3 and MOF in Drosophila S2 cells

(Submitter supplied) ChIP-chip profiles of MLE, MSL3 and MOF in Drosophila S2 cells
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7107
10 Samples
Download data: PAIR
Series
Accession:
GSE37863
ID:
200037863
17.

RNA-seq data in WT, roX1, roX2, roX1roX2 mutants in D. melanogaster

(Submitter supplied) Study of single and double mutants of the two roX RNAs in D. melanogaster
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17275
13 Samples
Download data: TXT, XLSX
Series
Accession:
GSE115779
ID:
200115779
18.

 RNA-Sequencing data from PofD119, Zhr1, PoX2Df1.688 and Oregon-R adult Drosophila melanogaster (Females and Males, separately).

(Submitter supplied) The prominent role of pericentromeric Mbp block of 1.688 satellites in hybrid incompatibility, facilitating role of distributed X-linked 1.688 satellites in dosage compensation in males and being as a necessary element for POF recruitment to chromosome X in females led us to further investigate the role of 1.688 satellites and POF in chromosome-wide gene regulation by comparing RNA-seq data from the relevant mutants in comparison to wildtype.
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17275
32 Samples
Download data: TXT
Series
Accession:
GSE136637
ID:
200136637
19.

GAF is essential for zygotic genome activation and chromatin accessibility in the early Drosophila embryo

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL21306 GPL19132 GPL25244
50 Samples
Download data
Series
Accession:
GSE152773
ID:
200152773
20.

GAF is essential for zygotic genome activation and chromatin accessibility in the early Drosophila embryo [RNA-seq]

(Submitter supplied) Following fertilization, the genomes of the germ cells are reprogrammed to form the totipotent embryo. Pioneer transcription factors are essential for remodeling the chromatin and driving the initial wave of zygotic gene expression. In Drosophila melanogaster, the pioneer factor Zelda is essential for development through this dramatic period of reprogramming, known as the maternal- to-zygotic transition (MZT). more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19132
6 Samples
Download data: TXT
Series
Accession:
GSE152772
ID:
200152772
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