Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7701
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dc.contributor.authorGUNGI, AKHILAen_US
dc.contributor.authorSaha, Shagniken_US
dc.contributor.authorPAL, MRINMOYen_US
dc.contributor.authorGALANDE, SANJEEVen_US
dc.date.accessioned2023-04-19T06:48:08Z
dc.date.available2023-04-19T06:48:08Z
dc.date.issued2023-05en_US
dc.identifier.citationLife Science Alliance, 6(5), e202201619.en_US
dc.identifier.issn2575-1077en_US
dc.identifier.urihttps://doi.org/10.26508/lsa.202201619en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7701
dc.description.abstractThe evolution of the first body axis in the animal kingdom and its extensive ability to regenerate makes Hydra, a Cnidarian, an excellent model system for understanding the underlying epigenetic mechanisms. We identify that monomethyltransferase SETD8 is critical for regeneration in Hydra because of its conserved interaction with β-catenin to fine-tune the associated gene regulatory network. Inhibition of SETD8 activity abolishes head and foot regeneration in Hydra. Furthermore, we show that H4K20me1, the histone mark imparted by SETD8, colocalizes with the transcriptional activation machinery locally at the β-catenin-bound TCF/LEF-binding sites on the promoters of head-associated genes, marking an epigenetic activation mode. In contrast, genome-wide analysis of the H4K20me1 occupancy revealed a negative correlation with transcriptional activation. We propose that H4K20me1 acts as a general repressive histone mark in Cnidaria and describe its dichotomous role in transcriptional regulation in Hydra.en_US
dc.language.isoenen_US
dc.publisherLife Science Allianceen_US
dc.subjectBiologyen_US
dc.subject2023-MAR-WEEK4en_US
dc.subjectTOC-MAR-2023en_US
dc.subject2023en_US
dc.titleH4K20me1 plays a dual role in transcriptional regulation of regeneration and axis patterning in Hydraen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleLife Science Allianceen_US
dc.publication.originofpublisherForeignen_US
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