8354962

pubmed:Citation

6

We have identified a new truncation of apoB in a large kindred with hypobetalipoproteinemia that arose by an ambiguous deletion of one of four different groups of base-pairs. Eleven affected members of the kindred had total cholesterols (C) of 114 +/- 28, LDL-Cs of 46 +/- 21, and apoBs of 47 +/- 25 (all in mg/dl, mean +/- SD). These levels were lower (P < 0.0001) than in 15 unaffected relatives. On Western blotting, apoB-100 and a second major band corresponding to apoB-52 were seen in the affected individuals. The majority of the plasma apoB-52 was associated with a smaller than normal low density lipoprotein (LDL) particle. The molecular basis for this apoB-52 truncation is a 5-bp deletion, converting the sequence between cDNA nucleotide 7276 and 7283 from 5'-AAGTTAAG-3' into the mutant sequence 5'-AAG-3'. This results in a frameshift starting at amino acid residue 2357 and a termination codon at amino acid residue 2362. Deletion of one of four different groups of five consecutive bases, i.e., AAGTT, AGTTA, GTTAA, and TTAAG, all result in the same mutant sequence. Thus, the precise deletion is ambiguous. We propose that a misaligned pairing mechanism involving repeat sequences is compatible with this deletion mutation. We have noted similar ambiguous deletions associated with apoB-37, apoB-40, and a number of single base deletions and some may also be explained by a misaligned pairing mechanism. Small ambiguous deletions appear to constitute a major proportion of the apoB gene mutation spectrum suggesting that it may be a suitable model for studying the mechanisms of such mutations.

eng

IM

MEDLINE

0022-2275

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NLM

971-81

pubmed-meshheading:8354962-Adolescent, pubmed-meshheading:8354962-Adult, pubmed-meshheading:8354962-Aged, pubmed-meshheading:8354962-Aged, 80 and over, pubmed-meshheading:8354962-Amino Acid Sequence, pubmed-meshheading:8354962-Apolipoproteins B, pubmed-meshheading:8354962-Base Sequence, pubmed-meshheading:8354962-Child, pubmed-meshheading:8354962-Child, Preschool, pubmed-meshheading:8354962-Deoxyribonucleases, Type II Site-Specific, pubmed-meshheading:8354962-Female, pubmed-meshheading:8354962-Frameshift Mutation, pubmed-meshheading:8354962-Humans, pubmed-meshheading:8354962-Hypobetalipoproteinemias, pubmed-meshheading:8354962-Male, pubmed-meshheading:8354962-Middle Aged, pubmed-meshheading:8354962-Molecular Sequence Data, pubmed-meshheading:8354962-Pedigree, pubmed-meshheading:8354962-Repetitive Sequences, Nucleic Acid, pubmed-meshheading:8354962-Sequence Deletion

Apolipoprotein B-52 mutation associated with hypobetalipoproteinemia is compatible with a misaligned pairing deletion mechanism.

Journal Article, Research Support, U.S. Gov't, P.H.S.