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Publication : Human apolipoprotein B: chromosomal mapping and DNA polymorphisms of hepatic and intestinal species.

First Author  Mehrabian M Year  1986
Journal  Somat Cell Mol Genet Volume  12
Issue  3 Pages  245-54
PubMed ID  3012797 Mgi Jnum  J:8314
Mgi Id  MGI:56782 Doi  10.1007/BF01570783
Citation  Mehrabian M, et al. (1986) Human apolipoprotein B: chromosomal mapping and DNA polymorphisms of hepatic and intestinal species. Somat Cell Mol Genet 12(3):245-54
abstractText  Apolipoprotein B (apoB) is the major protein component of low-density and very-low-density lipoproteins. We have recently isolated nonoverlapping cDNA clones for apoB and confirmed their identity by sequence comparisons. We now report the mapping of the human apoB gene (APOB) to the p23-p24 region of chromosome 2 by examination of human-mouse somatic cell hybrids and by in situ hybridization to human chromosomes. Thus, APOB is unlinked to members of the dispersed gene family encoding other apolipoprotein species or to the gene encoding the low-density lipoprotein receptor. Hybridization analysis with genomic DNA and liver and intestinal mRNA suggests that APOB encodes both the high-molecular-weight form of apoB (apoB100) incorporated into very-low-density lipoproteins in liver and the lower-molecular-weight form (apoB48) incorporated into chylomicrons in intestine. Restriction fragment length polymorphisms of APOB have been identified and should prove useful in examining the possibility that genetic variations of APOB are involved in dyslipoproteinemias and atherosclerosis.
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