Genetic factors controlling structure and expression of apolipoproteins B and E in mice.
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We report the identification and partial characterization of polymorphisms among inbred strains of mice affecting several aspects of the expression of apolipoproteins B and E (apoB and apoE), the major proteins of low density lipoproteins (LDL) and very low density lipoproteins (VLDL). These polymorphisms include differences in the levels of the lipoproteins and apolipoproteins on both chow and high fat diets, differences in their response to a high fat diet challenge, and differences in the relative levels of the two molecular weight species of apoB. Although most strains exhibited a large increase in plasma LDL and VLDL in response to a high fat diet, the levels of apoB and apoE mRNA were either unaffected or, in some cases, decreased slightly. Also, the levels of apoB and apoE mRNA were not correlated among strains with the levels of the apolipoproteins in plasma, suggesting that genetic control occurs primarily at the level of lipoprotein catabolism. Elucidation of the precise mechanisms involved in the differences will require genetic analysis. Toward this end, we have identified DNA polymorphisms for apoB and apoE and have used these in segregation analysis to determine the chromosomal locations of the apoB and apoE structural genes in mice. The gene for apoB, designated Apob, resides in the proximal region of chromosome 12 linked to genes for ribosomal RNA and aryl hydrocarbon hydroxylase. The gene for apoE, designated Apoe, is located on chromosome 7, linked to genes…
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Different mouse strains can have up to a four-fold difference in plasma apoE levels.
“Studies have shown that different mouse strains can have up to a four-fold difference in plasma apoE levels [36,37].”
From Measurement of apolipoprotein E and amyloid β clearance rates in the mouse brain using bolus stable isotope labeling (2012) · cites this paper as [36]
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Diet-induced hypercholesterolemia in mice: prevention by overexpression of LDL receptors
Yokode, M., Hammer, R. E., Ishibashi, S., Brown, M. S., & Goldstein, J. L. (1990) · Science · doi:10.1126/science.2244210 · Cited by 175 · see citing works
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- Authors
- Lusis, A. J., Taylor, B. A., Quon, D., Zollman, S., & LeBoeuf, R. C.
- Affiliations
- United States Department of Veterans Affairs (US)
- ORCID
- Lusis, A J
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1987-06
- Volume
- 262
- Issue
- 16
- Pages
- 7594-7604
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W1537961425
- Cited by
- 144
- References
- 2
- Citations by year
- 2025: 1 · 2023: 2 · 2018: 2 · 2016: 1 · 2014: 2 · 2012: 3
- FWCI
- 10.26
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- The Mouseion at the JAXlibrary (Jackson Laboratory) (submittedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL 27-481)
- National Institute of General Medical Sciences (GM 18684)
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Keywords
- apolipoprotein B, apolipoprotein E, genetic polymorphism, inbred mouse strains, low-density lipoprotein, VLDL, high-fat diet, gene mapping, chromosome 12, chromosome 7, lipoprotein catabolism, mRNA expression, diet-induced atherosclerosis, apolipoprotein A-I, apolipoprotein A-II, genetic linkage
- MeSH terms
- Animals, Apolipoproteins B, Apolipoproteins E, Cholesterol, Cloning, Molecular, DNA, DNA Restriction Enzymes, Female, Gene Expression Regulation, Genes, Mice, Inbred Strains, Nucleic Acid Hybridization, RNA, Messenger, Species Specificity, Transcription, Genetic, Mice
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