Changes in levels of transcription can be difficult to gauge in animals with lethal mutations. For example, mutations in a regulatory region of an essential gene can have secondary consequences that complicate attempts to quantify the transcripts produced by the mutant gene. We describe a method that circumvents this problem by revealing the relative amount of transcript produced from each allele in a heterozygote. With this method, recessive lethal mutations can be analyzed in animals that are phenotypically wild type. We used this technique to analyze mutations in the regulatory region of the Drosophila engrailed gene and found that truncations reduce transcription to levels that depend both upon the tissue and upon the location of the chromosomal break. We also found that these mutations affect expression of the linked invected gene, suggesting that engrailed and invected share a complex set of regulatory elements that operate over at least 85 kb. We suggest that this technique will have general utility for the quantitation of allele-specific transcripts, even when amounts of tissue are limiting.
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http://dx.doi.org/10.1073/pnas.91.26.12696 | DOI Listing |
Development
December 2024
Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
More than 40 years ago, studies of the Drosophila engrailed and Hox genes led to major discoveries that shaped the history of developmental biology. We learned that these genes define the state of determination of cells that populate particular spatially defined regions: the identity of segmental domains by Hox genes, and the identity of posterior developmental compartments by engrailed. Hence, the boundaries that delimit spatial domains depend on engrailed.
View Article and Find Full Text PDFbioRxiv
May 2024
Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
For a damaged tissue to regenerate, the injured site must repair the wound, proliferate, and restore the correct patterning and cell types. We found that Zelda, a pioneer transcription factor largely known for its role in embryonic zygotic genome activation, is dispensable for normal wing development but crucial for wing disc patterning during regeneration. Impairing Zelda function during disc regeneration resulted in adult wings with a plethora of cell fate errors, affecting the veins, margins, and posterior compartment identity.
View Article and Find Full Text PDFPLoS Genet
November 2023
Division of Developmental Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
engrailed (en) encodes a homeodomain transcription factor crucial for the proper development of Drosophila embryos and adults. Like many developmental transcription factors, en expression is regulated by many enhancers, some of overlapping function, that drive expression in spatially and temporally restricted patterns. The en embryonic enhancers are located in discrete DNA fragments that can function correctly in small reporter transgenes.
View Article and Find Full Text PDFNat Commun
September 2023
Centro Andaluz de Biología del Desarrollo (CABD), CSIC-JA-UPO Ctra. de Utrera, km1, 41013, Seville, Spain.
The re-use of genes in new organs forms the base of many evolutionary novelties. A well-characterised case is the recruitment of the posterior spiracle gene network to the Drosophila male genitalia. Here we find that this network has also been co-opted to the testis mesoderm where is required for sperm liberation, providing an example of sequentially repeated developmental co-options.
View Article and Find Full Text PDFInsects
August 2023
Molecular and Cellular Biology, University of Arizona, Tucson, AZ 85721, USA.
and encode paralogous transcription factors found as a closely linked tandem duplication within holometabolous insects. mutants segment normally, then fail to maintain their segments. Loss of is viable, while loss of both genes results in asegmental larvae.
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