4.3 Article

Genomic organization of the autonomous regulatory domain of eyeless locus in Drosophila melanogaster

Journal

G3-GENES GENOMES GENETICS
Volume 11, Issue 12, Pages -

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/g3journal/jkab338

Keywords

eyeless; chromatin domain boundary; polycomb response elements; matrix-associated regions; long-range interaction; chromatin domain; gene regulation; Drosophila

Funding

  1. Council of Scientific and Industrial Research (CSIR), India

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The study reveals distinct spatial and temporal expression patterns of the eyeless gene in Drosophila compared to its flanking genes, maintained through boundary elements ME and EB. The functional autonomy and insulation of the ey locus from neighboring regions is suggested. Additionally, a new Polycomb Response Element, ey-PRE, is identified to help maintain the expression state of the ey gene during early development.
In Drosophila, expression of eyeless (ey) gene is restricted to the developing eyes and central nervous system. However, the flanking genes, myoglianin (myo), and bent (bt) have different temporal and spatial expression patterns as compared to the ey. How distinct regulation of ey is maintained is mostly unknown. Earlier, we have identified a boundary element intervening myo and ey genes (ME boundary) that prevents the crosstalk between the cis-regulatory elements of myo and ey genes. In the present study, we further searched for the ciselements that define the domain of ey and maintain its expression pattern. We identify another boundary element between ey and bt, the EB boundary. The EB boundary separates the regulatory landscapes of ey and bt genes. The two boundaries, ME and EB, show a longrange interaction as well as interact with the nuclear architecture. This suggests functional autonomy of the ey locus and its insulation from differentially regulated flanking regions. We also identify a new Polycomb Response Element, the ey-PRE, within the ey domain. The expression state of the ey gene, once established during early development is likely to be maintained with the help of ey-PRE. Our study proposes a general regulatory mechanism by which a gene can be maintained in a functionally independent chromatin domain in gene-rich euchromatin.

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