Javascript must be enabled to continue!
Functional mapping of the mouse hairless gene promoter region
View through CrossRef
Abstract
The mouse
hairless
gene (
Hr
) encodes a protein of 127 kDa, acting as corepressor of nuclear hormone receptors. The Hairless protein (HR) is involved in the control of the cellular transition to the first hair cycle in adult Mammals. In its absence hair follicles disintegrate leading to a complete and irreversible hair loss with formation of cutaneous cysts. The hairless phenotype is therefore linked to defective proliferation and migration of the hair follicle stem cells apparently unable to respond to various signalling molecules. The
Hr
gene is expressed at high levels in skin and brain, and
hairless
transcripts were detected in gonads, thymus and colon. Although the patterns of
Hr
expression appear to be spatially and temporally regulated, very little is known about the molecular basis of the transcriptional control underlying
Hr
gene function. In this work we determine the precise transcriptional initiation start site of the mouse
Hr
gene and identify a new 1,1 kb cis-control element (RE1) that encompasses the promoter region and is able to drive luciferase reporter expression in skin and brain derived cell lines. We performed a deletion analysis and explored functionally regulatory motifs within this fragment to show that the role of this upstream regulatory region is linked to the presence of TRE and VDRE binding sites. We find that a TRE situated at –300 bp from the cap site is essential for gene expression in both skin NIH 3T3 and GHFT1 cells, while a VDRE positioned 94 bp upstream of the TRE modulates reporter expression specifically in skin derived cell lines. In addition, we define a novel cis-regulatory motif UE60, situated at the 5’-end of RE1 and likely to interact with both TRE and VDRE. Our data complete previous results on the possible existence of an autoregulatory pathway, implicated in
Hr
gene regulation. Taken together these findings reveal a complex molecular network that potentially links several signalling pathways in hair follicle formation. We discuss the organisation of the regulatory modules in the mouse
Hr
gene upstream DNA sequences in the light of the high homology of this region in mouse, rat and human.
Title: Functional mapping of the mouse
hairless
gene promoter region
Description:
Abstract
The mouse
hairless
gene (
Hr
) encodes a protein of 127 kDa, acting as corepressor of nuclear hormone receptors.
The Hairless protein (HR) is involved in the control of the cellular transition to the first hair cycle in adult Mammals.
In its absence hair follicles disintegrate leading to a complete and irreversible hair loss with formation of cutaneous cysts.
The hairless phenotype is therefore linked to defective proliferation and migration of the hair follicle stem cells apparently unable to respond to various signalling molecules.
The
Hr
gene is expressed at high levels in skin and brain, and
hairless
transcripts were detected in gonads, thymus and colon.
Although the patterns of
Hr
expression appear to be spatially and temporally regulated, very little is known about the molecular basis of the transcriptional control underlying
Hr
gene function.
In this work we determine the precise transcriptional initiation start site of the mouse
Hr
gene and identify a new 1,1 kb cis-control element (RE1) that encompasses the promoter region and is able to drive luciferase reporter expression in skin and brain derived cell lines.
We performed a deletion analysis and explored functionally regulatory motifs within this fragment to show that the role of this upstream regulatory region is linked to the presence of TRE and VDRE binding sites.
We find that a TRE situated at –300 bp from the cap site is essential for gene expression in both skin NIH 3T3 and GHFT1 cells, while a VDRE positioned 94 bp upstream of the TRE modulates reporter expression specifically in skin derived cell lines.
In addition, we define a novel cis-regulatory motif UE60, situated at the 5’-end of RE1 and likely to interact with both TRE and VDRE.
Our data complete previous results on the possible existence of an autoregulatory pathway, implicated in
Hr
gene regulation.
Taken together these findings reveal a complex molecular network that potentially links several signalling pathways in hair follicle formation.
We discuss the organisation of the regulatory modules in the mouse
Hr
gene upstream DNA sequences in the light of the high homology of this region in mouse, rat and human.
Related Results
The emergence and evolution of gene expression in genome regions replete with regulatory motifs
The emergence and evolution of gene expression in genome regions replete with regulatory motifs
Abstract
Gene regulation is essential for life and controlled by regulatory DNA. Mutations can modify the activity of regulatory DNA, and also create new regulatory...
Characterization of β-Actin Promoter from Nile Tilapia (Oreochromis niloticus)
Characterization of β-Actin Promoter from Nile Tilapia (Oreochromis niloticus)
<p>Promoter is one of the factors determining the successful of transgenesis. In this study we isolated and characterized β-actin promoter from Nile tilapia (tiBP) towards p...
Only a subset of the binary cell fate decisions mediated by Numb/Notch signaling in Drosophila sensory organ lineage requires Suppressor of Hairless
Only a subset of the binary cell fate decisions mediated by Numb/Notch signaling in Drosophila sensory organ lineage requires Suppressor of Hairless
ABSTRACT
In Drosophila, an adult external sensory organ (bristle) consists of four distinct cells which arise from a sensory organ precursor cell via two rounds of a...
Hair growth in skin grafts placed on hairless mice
Hair growth in skin grafts placed on hairless mice
AbstractThe purpose of this study is to investigate the possibility that hair growth is triggered by the loss of a specific hair follicle inhibitor.If the loss of an inhibitor is a...
Molecular prognostication of thyroid tumors : with special focus on TERT
Molecular prognostication of thyroid tumors : with special focus on TERT
<p dir="ltr">Thyroid carcinoma is the most common endocrine malignancy, with its incidence steadily increasing worldwide. These tumors can be challenging to diagnose, and tre...
Molecular prognostication of thyroid tumors : with special focus on TERT
Molecular prognostication of thyroid tumors : with special focus on TERT
<p dir="ltr">Thyroid carcinoma is the most common endocrine malignancy, with its incidence steadily increasing worldwide. These tumors can be challenging to diagnose, and tre...
Genomic and transcriptomic analyses provide new insights into the complex impacts of bud mutation in peach
Genomic and transcriptomic analyses provide new insights into the complex impacts of bud mutation in peach
Abstract
Bud mutation is an important solution in fruit breeding, but the mechanism of bud mutation remains largely unknown. Here, we present the phenotypic, genomic, and...
Expression and polymorphism of genes in gallstones
Expression and polymorphism of genes in gallstones
ABSTRACT
Through the method of clinical case control study, to explore the expression and genetic polymorphism of KLF14 gene (rs4731702 and rs972283) and SR-B1 gene...

