The activity of engrailed imaginal disc enhancers is modulated epigenetically by chromatin and autoregulation.

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...

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Main Authors: Yuzhong Cheng, Fountane Chan, Judith A Kassis
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-11-01
Series:PLoS Genetics
Online Access:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1010826&type=printable
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author Yuzhong Cheng
Fountane Chan
Judith A Kassis
author_facet Yuzhong Cheng
Fountane Chan
Judith A Kassis
author_sort Yuzhong Cheng
collection DOAJ
description 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. In contrast, the en imaginal disc enhancers (IDEs) do not function correctly in small reporter transgenes. En is expressed in the posterior compartment of wing imaginal discs; in contrast, small IDE-reporter transgenes are expressed mainly in the anterior compartment. We found that En binds to the IDEs and suggest that it may directly repress IDE function and modulate En expression levels. We identified two en IDEs, O and S. Deletion of either of these IDEs from a 79kb HA-en rescue transgene (HAen79) caused a loss-of-function en phenotype when the HAen79 transgene was the sole source of En. In contrast, flies with a deletion of the same IDEs from an endogenous en gene had no phenotype, suggesting a resiliency not seen in the HAen79 rescue transgene. Inserting a gypsy insulator in HAen79 between en regulatory DNA and flanking sequences strengthened the activity of HAen79, giving better function in both the ON and OFF transcriptional states. Altogether our data suggest that the en IDEs stimulate expression in the entire imaginal disc, and that the ON/OFF state is set by epigenetic memory set by the embryonic enhancers. This epigenetic regulation is similar to that of the Ultrabithorax IDEs and we suggest that the activity of late-acting enhancers in other genes may be similarly regulated.
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spelling doaj.art-9403f02556b44061958a61976787c53c2023-12-16T05:31:31ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042023-11-011911e101082610.1371/journal.pgen.1010826The activity of engrailed imaginal disc enhancers is modulated epigenetically by chromatin and autoregulation.Yuzhong ChengFountane ChanJudith A Kassisengrailed (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. In contrast, the en imaginal disc enhancers (IDEs) do not function correctly in small reporter transgenes. En is expressed in the posterior compartment of wing imaginal discs; in contrast, small IDE-reporter transgenes are expressed mainly in the anterior compartment. We found that En binds to the IDEs and suggest that it may directly repress IDE function and modulate En expression levels. We identified two en IDEs, O and S. Deletion of either of these IDEs from a 79kb HA-en rescue transgene (HAen79) caused a loss-of-function en phenotype when the HAen79 transgene was the sole source of En. In contrast, flies with a deletion of the same IDEs from an endogenous en gene had no phenotype, suggesting a resiliency not seen in the HAen79 rescue transgene. Inserting a gypsy insulator in HAen79 between en regulatory DNA and flanking sequences strengthened the activity of HAen79, giving better function in both the ON and OFF transcriptional states. Altogether our data suggest that the en IDEs stimulate expression in the entire imaginal disc, and that the ON/OFF state is set by epigenetic memory set by the embryonic enhancers. This epigenetic regulation is similar to that of the Ultrabithorax IDEs and we suggest that the activity of late-acting enhancers in other genes may be similarly regulated.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1010826&type=printable
spellingShingle Yuzhong Cheng
Fountane Chan
Judith A Kassis
The activity of engrailed imaginal disc enhancers is modulated epigenetically by chromatin and autoregulation.
PLoS Genetics
title The activity of engrailed imaginal disc enhancers is modulated epigenetically by chromatin and autoregulation.
title_full The activity of engrailed imaginal disc enhancers is modulated epigenetically by chromatin and autoregulation.
title_fullStr The activity of engrailed imaginal disc enhancers is modulated epigenetically by chromatin and autoregulation.
title_full_unstemmed The activity of engrailed imaginal disc enhancers is modulated epigenetically by chromatin and autoregulation.
title_short The activity of engrailed imaginal disc enhancers is modulated epigenetically by chromatin and autoregulation.
title_sort activity of engrailed imaginal disc enhancers is modulated epigenetically by chromatin and autoregulation
url https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1010826&type=printable
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