Frontabdominal-7, Fab-7 PRE
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Fab-7 using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
JBrowse - Visual display of RNA-Seq signals
View Dmel\Fab-7 in JBrowsePlease Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.
For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.
Fab-7 sites exhibit epigenetic inheritance of depressed chromatin states.
Fab-7 can be switched to an active or a silencing mode. Both epigenetically determined states can be transmitted to a fraction of progeny in the next generation through the female germline. This suggests that a protein-based cellular memory mechanism can be propogated through meiosis.
iab-7 PRE.
The Fab-7 region can be subdivided into a chromatin domain boundary and a Polycomb-response element.
Deletion of the Fab-7 element results in fusion of the iab-6 and iab-7 cis-regulatory domains into a single regulatory domain that inappropriately regulates Abd-B. This result suggests Fab-7 is a chromatin domain boundary within the context of the bithorax complex that normally functions to ensure the autonomous activity of the iab-6 and iab-7 cis-regulatory domains.
A specialised DNA element, Fab-7, is proposed to function as a boundary element that separates the iab-6 and iab-7 cis regulatory regions within the Abd-B domain of the BX-C. Studies suggest Fab-7 functions as an attenuator which weakens gene expression by reducing enhancer-promoter interactions. Fab-7 selectively blocks distal enhancers in an orientation-independent fashion and can function when far from either the distal enhancer or target promoter.
The role of Fab-7 as a boundary element may be restricted to particular tissues in which the homeotic genes are active.
The sequence and chromatin organisation of Fab-7 and Mcp have been compared.
The expression of the P{bluetail} insertion into the PS12-specific regulatory domain in Abd-Bblt allows dissection of the neighboring cis-regulatory region into independent domains.
Boundary elements in the bithorax complex, such as Fab-7 organize the parasegment specific cis-regulatory sub-regions into a series of autonomous domains, insulating each domain from the regulatory influences of the adjacent ones.
An insulating boundary element in the 'Fab7' region is characterized by an unusual chromatin structure.
Fab-7 and Mcp region chromatin structure contain distinct chromatin structures that display similarities to the scs and scs' structures of the Hsp70A locus, and are constitutive. Deletion analysis demonstrates that the DNA segment required for Fab-7 function contains 3 nuclease hypersensitive regions and that for Mcp function contains 1 major hypersensitive region and 3 minor nuclease hypersensitive regions.