Literature DB >> 2895796

ApoB gene MspI RFLP in exon 26 changes amino acid 3611 from Arg to Gln.

L S Huang1, J de Graaf, J L Breslow.   

Abstract

An apolipoprotein B gene MspI RFLP was identified by the use of a probe to a portion of the 3' end of the gene. By Southern blotting analysis after digestion with MspI, this probe detected either a 9 kb or a 2.6 kb fragment. Family studies showed that these corresponded to alleles that segregated in a simple Mendelian fashion. The minor allele (9.0 kb) had a frequency of approximately 12% in an unrelated Caucasian population. Restriction mapping showed that the minor allele was due to the loss of an MspI site in exon 26. Sequencing of both alleles in the region containing the polymorphic MspI site revealed a single-base pair alteration which abolished the MspI site at codon 3611 of the mature apoB protein. In the major allele, this codon is CGG, which specifies Arg; whereas in the minor allele, it was CAG, which codes for Gln.

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Year:  1988        PMID: 2895796

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  7 in total

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Authors:  G Breguet; R Bütler; E Bütler-Brunner; A Sanchez-Mazas
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

2.  Apolipoprotein B amino acid 3611 substitution from arginine to glutamine creates the Ag (h/i) epitope: the polymorphism is not associated with differences in serum cholesterol and apolipoprotein B levels.

Authors:  C F Xu; N Nanjee; M J Tikkanen; J K Huttunen; P Pietinen; R Bütler; F Angelico; M Del Ben; B Mazzarella; R Antonio
Journal:  Hum Genet       Date:  1989-07       Impact factor: 4.132

3.  Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100.

Authors:  L F Soria; E H Ludwig; H R Clarke; G L Vega; S M Grundy; B J McCarthy
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

4.  Molecular and metabolic basis for the metabolic disorder normotriglyceridemic abetalipoproteinemia.

Authors:  D A Hardman; C R Pullinger; R L Hamilton; J P Kane; M J Malloy
Journal:  J Clin Invest       Date:  1991-11       Impact factor: 14.808

5.  Exclusion of linkage between the human apolipoprotein B gene and abetalipoproteinemia.

Authors:  L S Huang; P A Jänne; J de Graaf; M Cooper; R J Deckelbaum; H Kayden; J L Breslow; R J Decklebaum
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

6.  Genome-Wide Association Analysis for Blood Lipid Traits Measured in Three Pig Populations Reveals a Substantial Level of Genetic Heterogeneity.

Authors:  Hui Yang; Xiaochang Huang; Zhijun Zeng; Wanchang Zhang; Chenlong Liu; Shaoming Fang; Lusheng Huang; Congying Chen
Journal:  PLoS One       Date:  2015-06-29       Impact factor: 3.240

7.  Genetic association of APOB polymorphisms with variation in serum lipid profile among the Kuwait population.

Authors:  Suzanne A Al-Bustan; Majed A Alnaqeeb; Babitha G Annice; Ghada A Ebrahim; Thanaa M Refai
Journal:  Lipids Health Dis       Date:  2014-10-08       Impact factor: 3.876

  7 in total

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