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PMID: 8128959 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Age-related human mtDNA deletions: a heterogeneous set of deletions arising at a single pair of directly repeated sequences.

American journal of human genetics ·Vol. 54 ·No. 4 ·1994-04-00 ·Pages 618-30

Baumer A, Zhang C, Linnane AW, Nagley P

Abstract

Deletions in mtDNA accumulate during the human aging process, arising from either intramolecular illegitimate recombination or strand slippage during replication, which results in subgenomic mtDNA molecules. We identify here two classes of mtDNA deletions--class A deletions, which are homogeneous at the breakpoints, with all subgenomic molecules therefore being identical in size, and class B deletions, which arise from a less stringent process that gives rise to heterogeneity at the breakpoints, with the subgenomic molecules being of slightly different sizes. A novel approach is described that offers a global overview of the populations of different deletions in individual tissues. It is based on PCR cycle-sequencing reactions that are carried out directly on mtDNA segments, amplified by PCR from total cellular DNA. The results show a clear size homogeneity of the subgenomic mtDNA molecules representative of class A, which carry a commonly detected 4,977-bp deletion occurring at a pair of 13-bp directly repeated sequences. In this case, precisely one copy of the repeat is retained in the subgenomic molecules. We then describe a class B situation comprising a family of at least nine closely related 8.04-kb deletions involving the same pair of 5-bp direct repeats. In this situation, the breakpoints differ at the base-pair level (8,037-8,048-bp deletions); the subgenomic molecules retain > 1 copy, 1 copy, or < 1 copy of the 5-bp repeat. In different tissues from either the same individual or among different individuals, there is a widely variable occurrence of particular deletions in the subgenomic mtDNA population within this class B set. Class B deletions offer a new approach for studying the accumulation of mtDNA deletions, thereby providing insight into the independent somatic origin of mutated mtDNA molecules, both in aging and in mitochondrial diseases. We also report a convenient method for ascertaining whether a given PCR product results from the amplification of a subgenomic mtDNA template, on the basis of the selective degradation of full-length mtDNA molecules prior to PCR.

MeSH Terms
Adult Aged Aged, 80 and over Aging/genetics Base Sequence DNA Mutational Analysis DNA, Mitochondrial/genetics Humans Middle Aged Mitochondria, Heart Mitochondria, Muscle Molecular Sequence Data Organ Specificity Polymerase Chain Reaction/methods Repetitive Sequences, Nucleic Acid Sequence Deletion
Chemicals
DNA, Mitochondrial
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Baumer A
Department of Biochemistry, Monash University, Clayton, Victoria, Australia.
Zhang C
Linnane A W
Nagley P
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35 references, click to expand
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1994-04-00
Pages
618-30
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1918099
Subset
IM
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