4.4 Article

Spatial expression of transcription factors in Drosophila embryonic organ development

期刊

GENOME BIOLOGY
卷 14, 期 12, 页码 -

出版社

BMC
DOI: 10.1186/gb-2013-14-12-r140

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资金

  1. NIH NRSA postdoctoral fellowship
  2. NHGRI [1U01HG007031-01]
  3. Center for Science of Information (CSoI), an NSF Science and Technology Center [CCF-0939370]
  4. NIH [R01 GM076655, R01 GM097231]
  5. Department of Energy [DEAC02-05CH11231]
  6. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [R01HG004037, U01HG007031] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM097231, R01GM076655] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS054814] Funding Source: NIH RePORTER
  9. Direct For Biological Sciences [0644282] Funding Source: National Science Foundation

向作者/读者索取更多资源

Background: Site-specific transcription factors (TFs) bind DNA regulatory elements to control expression of target genes, forming the core of gene regulatory networks. Despite decades of research, most studies focus on only a small number of TFs and the roles of many remain unknown. Results: We present a systematic characterization of spatiotemporal gene expression patterns for all known or predicted Drosophila TFs throughout embryogenesis, the first such comprehensive study for any metazoan animal. We generated RNA expression patterns for all 708 TFs by in situ hybridization, annotated the patterns using an anatomical controlled vocabulary, and analyzed TF expression in the context of organ system development. Nearly all TFs are expressed during embryogenesis and more than half are specifically expressed in the central nervous system. Compared to other genes, TFs are enriched early in the development of most organ systems, and throughout the development of the nervous system. Of the 535 TFs with spatially restricted expression, 79% are dynamically expressed in multiple organ systems while 21% show single-organ specificity. Of those expressed in multiple organ systems, 77 TFs are restricted to a single organ system either early or late in development. Expression patterns for 354 TFs are characterized for the first time in this study. Conclusions: We produced a reference TF dataset for the investigation of gene regulatory networks in embryogenesis, and gained insight into the expression dynamics of the full complement of TFs controlling the development of each organ system.

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