Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Chromosomal localization, genomic organization, and developmental expression of the murine caveolin gene family (Cav‐1, ‐2, and ‐3)

View through CrossRef
Caveolins (Cav‐1, ‐2, and ‐3) are a gene family of cytoplasmic membrane‐anchored scaffolding proteins that: (i) help to sculpt caveolae membranes from the plasma membrane proper; and (ii) participate in the sequestration of inactive signaling molecules. In the adult, caveolin‐1 and ‐2 are co‐expressed and are most abundant in type I pneumocytes, endothelia, fibroblastic cells and adipocytes, while the expression of caveolin‐3 is restricted to striated muscle cells. However, little is known regarding the genomic organization and developmental expression of the caveolin gene family. Here, using the mouse as a model system, we examine the chromosomal localization, the detailed intron‐exon organization, and developmental expression pattern of the caveolin gene family. cDNAs encoding caveolin‐1, ‐2, and ‐3 were used as probes to isolate murine genomic clones containing these genes. Fluorescence in situ hybridization (FISH) analysis using these genomic clones as probes reveals that all three caveolin genes are localized to murine chromosome 6. Specifically, caveolin‐1 and ‐2 co‐localize to chromosomal region 6‐A2, while caveolin‐3 is located within the chromosomal region 6‐E1. Searches of the NCBI Human/Mouse Homology map indicate that murine region 6‐A2 corresponds to human chromosome 7q31. As this region (6‐A2/7q31) is the site of an as yet unidentified tumor suppressor gene(s), our mapping studies clearly define caveolin‐1 and caveolin‐2 as candidate genes that may be deleted at these loci. All three caveolin genes show similar intron‐exon organization, with the last exon of each gene encoding the bulk of the known caveolin functional domains. The boundary position of the last exon is essentially identical in all three caveolin genes, suggesting that they may have arisen through gene duplication events. Developmentally, all three caveolins were expressed late during mouse embryogenesis as assessed by Northern and Western blot analysis. We examined the localization of the caveolin proteins in sections of day 16 mouse embryos using a well‐characterized panel of antibody probes. Caveolin‐1 and ‐2 were most abundantly expressed in the developing lung parenchyma, while caveolin‐3 was most abundantly expressed in developing tissues that consist primarily of skeletal muscle cells. As the expression of all three caveolins in the adult is highest in terminally differentiated cell types, this is consistent with the idea that caveolins may be viewed as late markers of differentiation during embryogenesis.
Title: Chromosomal localization, genomic organization, and developmental expression of the murine caveolin gene family (Cav‐1, ‐2, and ‐3)
Description:
Caveolins (Cav‐1, ‐2, and ‐3) are a gene family of cytoplasmic membrane‐anchored scaffolding proteins that: (i) help to sculpt caveolae membranes from the plasma membrane proper; and (ii) participate in the sequestration of inactive signaling molecules.
In the adult, caveolin‐1 and ‐2 are co‐expressed and are most abundant in type I pneumocytes, endothelia, fibroblastic cells and adipocytes, while the expression of caveolin‐3 is restricted to striated muscle cells.
However, little is known regarding the genomic organization and developmental expression of the caveolin gene family.
Here, using the mouse as a model system, we examine the chromosomal localization, the detailed intron‐exon organization, and developmental expression pattern of the caveolin gene family.
cDNAs encoding caveolin‐1, ‐2, and ‐3 were used as probes to isolate murine genomic clones containing these genes.
Fluorescence in situ hybridization (FISH) analysis using these genomic clones as probes reveals that all three caveolin genes are localized to murine chromosome 6.
Specifically, caveolin‐1 and ‐2 co‐localize to chromosomal region 6‐A2, while caveolin‐3 is located within the chromosomal region 6‐E1.
Searches of the NCBI Human/Mouse Homology map indicate that murine region 6‐A2 corresponds to human chromosome 7q31.
As this region (6‐A2/7q31) is the site of an as yet unidentified tumor suppressor gene(s), our mapping studies clearly define caveolin‐1 and caveolin‐2 as candidate genes that may be deleted at these loci.
All three caveolin genes show similar intron‐exon organization, with the last exon of each gene encoding the bulk of the known caveolin functional domains.
The boundary position of the last exon is essentially identical in all three caveolin genes, suggesting that they may have arisen through gene duplication events.
Developmentally, all three caveolins were expressed late during mouse embryogenesis as assessed by Northern and Western blot analysis.
We examined the localization of the caveolin proteins in sections of day 16 mouse embryos using a well‐characterized panel of antibody probes.
Caveolin‐1 and ‐2 were most abundantly expressed in the developing lung parenchyma, while caveolin‐3 was most abundantly expressed in developing tissues that consist primarily of skeletal muscle cells.
As the expression of all three caveolins in the adult is highest in terminally differentiated cell types, this is consistent with the idea that caveolins may be viewed as late markers of differentiation during embryogenesis.

Related Results

Hubungan Perilaku Pola Makan dengan Kejadian Anak Obesitas
Hubungan Perilaku Pola Makan dengan Kejadian Anak Obesitas
<p><em><span style="font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: EN-US; mso-fareast-langua...
On Flores Island, do "ape-men" still exist? https://www.sapiens.org/biology/flores-island-ape-men/
On Flores Island, do "ape-men" still exist? https://www.sapiens.org/biology/flores-island-ape-men/
<span style="font-size:11pt"><span style="background:#f9f9f4"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><b><spa...
Association between elevated Lp(a) and CAV in heart transplant recipients
Association between elevated Lp(a) and CAV in heart transplant recipients
AbstractBackgroundCardiac allograft vasculopathy (CAV) is the leading cause of late graft failure and mortality after heart transplantation (HT). Among non-HT patients, elevated Lp...
The TGF-β1/p53/PAI-1 Signaling Axis in Vascular Senescence: Role of Caveolin-1
The TGF-β1/p53/PAI-1 Signaling Axis in Vascular Senescence: Role of Caveolin-1
Stress-induced premature cellular senescence is a significant factor in the onset of age-dependent disease in the cardiovascular system. Plasminogen activator inhibitor-1 (PAI-1), ...
Single-cell RNA-sequencing identifies unique cell-specific gene expression profiles in high-grade cardiac allograft vasculopathy
Single-cell RNA-sequencing identifies unique cell-specific gene expression profiles in high-grade cardiac allograft vasculopathy
AbstractBackgroundCardiac allograft vasculopathy (CAV), a diffuse thickening of the intima of the coronary arteries and microvasculature, is the leading cause of late graft failure...
Loss of Caveolin-1 Impairs Light Flicker-Induced Neurovascular Coupling at the Optic Nerve Head
Loss of Caveolin-1 Impairs Light Flicker-Induced Neurovascular Coupling at the Optic Nerve Head
Glaucoma is a neurodegenerative disease, which results in characteristic visual field defects. Intraocular pressure (IOP) remains the main risk factor for this leading cause of bli...
Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells
Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells
AbstractTrastuzumab emtansine (T-DM1) is an antibody drug conjugate (ADC) that was recently approved for the treatment of HER-2-positive metastatic breast cancer. The drug sensitiv...

Back to Top