Alternative forms of the scavenger receptor BI (SR-BI)

The class B, type I scavenger receptor has been implicated as a receptor for high density lipoprotein (HDL). We have isolated a murine cDNA clone encoding an alternative form of SR-BI that differs in the putative cytoplasmic domain of the receptor. This variant form, likely the result of alternative...

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Main Authors: N R Webb, W J de Villiers, P M Connell, F C de Beer, D R van der Westhuyzen
Format: Article
Language:English
Published: Elsevier 1997-07-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520374319
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spelling doaj-7e27528ca9314ccfa3e283d176cc4d502021-04-26T05:48:26ZengElsevierJournal of Lipid Research0022-22751997-07-0138714901495Alternative forms of the scavenger receptor BI (SR-BI)N R Webb0W J de Villiers1P M Connell2F C de Beer3D R van der Westhuyzen4Department of Internal Medicine, University of Kentucky Medical Center, Lexington 40536, USA.Department of Internal Medicine, University of Kentucky Medical Center, Lexington 40536, USA.Department of Internal Medicine, University of Kentucky Medical Center, Lexington 40536, USA.Department of Internal Medicine, University of Kentucky Medical Center, Lexington 40536, USA.Department of Internal Medicine, University of Kentucky Medical Center, Lexington 40536, USA.The class B, type I scavenger receptor has been implicated as a receptor for high density lipoprotein (HDL). We have isolated a murine cDNA clone encoding an alternative form of SR-BI that differs in the putative cytoplasmic domain of the receptor. This variant form, likely the result of alternative mRNA splicing, is designated SR-BI.2. SR-BI.2 mRNA was detected in mouse tissues known to express SR-BI and tissue-specific differences in the relative abundance of SR-BI.2 were apparent. In mouse adrenal glands, SR-BI.2 represented approximately one-third of total SR-BI mRNA, whereas in mouse testes, SR-BI.2 represented the major mRNA species (79% of total). SR-BI.2 was also detected in the human cell lines examined, namely HeLa, HepG2, and THP-1 cells. CHO cells transfected with the mouse SR-BI.2 cDNA expressed significant levels of SR-BI.2 protein and acquired the ability to take up fluorescent lipid (DiI) from DiI-HDL. Alternative splicing of SR-BI represents a potentially important process for the regulation of SR-BI expression and function.http://www.sciencedirect.com/science/article/pii/S0022227520374319
collection DOAJ
language English
format Article
sources DOAJ
author N R Webb
W J de Villiers
P M Connell
F C de Beer
D R van der Westhuyzen
spellingShingle N R Webb
W J de Villiers
P M Connell
F C de Beer
D R van der Westhuyzen
Alternative forms of the scavenger receptor BI (SR-BI)
Journal of Lipid Research
author_facet N R Webb
W J de Villiers
P M Connell
F C de Beer
D R van der Westhuyzen
author_sort N R Webb
title Alternative forms of the scavenger receptor BI (SR-BI)
title_short Alternative forms of the scavenger receptor BI (SR-BI)
title_full Alternative forms of the scavenger receptor BI (SR-BI)
title_fullStr Alternative forms of the scavenger receptor BI (SR-BI)
title_full_unstemmed Alternative forms of the scavenger receptor BI (SR-BI)
title_sort alternative forms of the scavenger receptor bi (sr-bi)
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1997-07-01
description The class B, type I scavenger receptor has been implicated as a receptor for high density lipoprotein (HDL). We have isolated a murine cDNA clone encoding an alternative form of SR-BI that differs in the putative cytoplasmic domain of the receptor. This variant form, likely the result of alternative mRNA splicing, is designated SR-BI.2. SR-BI.2 mRNA was detected in mouse tissues known to express SR-BI and tissue-specific differences in the relative abundance of SR-BI.2 were apparent. In mouse adrenal glands, SR-BI.2 represented approximately one-third of total SR-BI mRNA, whereas in mouse testes, SR-BI.2 represented the major mRNA species (79% of total). SR-BI.2 was also detected in the human cell lines examined, namely HeLa, HepG2, and THP-1 cells. CHO cells transfected with the mouse SR-BI.2 cDNA expressed significant levels of SR-BI.2 protein and acquired the ability to take up fluorescent lipid (DiI) from DiI-HDL. Alternative splicing of SR-BI represents a potentially important process for the regulation of SR-BI expression and function.
url http://www.sciencedirect.com/science/article/pii/S0022227520374319
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