Literature DB >> 20151402

The acquisition of an inheritable 50-bp deletion in the human mtDNA control region does not affect the mtDNA copy number in peripheral blood cells.

Rui Bi1, A-Mei Zhang, Wen Zhang, Qing-Peng Kong, Bei-Ling Wu, Xiao-Hong Yang, Dong Wang, Yang Zou, Ya-Ping Zhang, Yong-Gang Yao.   

Abstract

The mitochondrial DNA (mtDNA) control region is believed to play an important biological role in mtDNA replication. Large deletions in this region are rarely found, but when they do occur they might be expected to interfere with the replication of the molecule, thus leading to a reduction of mtDNA copy number. During a survey for mtDNA sequence variations in 5,559 individuals from the general Chinese population and 2,538 individuals with medical disorders, we identified a 50-bp deletion (m.298_347del50) in the mtDNA control region in a member of a healthy Han Chinese family belonging to haplogroup B4c1b2, as suggested by complete mtDNA genome sequencing. This deletion removes the conserved sequence block II (CSBII; region 299-315) and the replication primer location (region 317-321). However, quantification of the mtDNA copy number in this subject showed a value within a range that was observed in 20 healthy subjects without the deletion. The deletion was detected in the hair samples of the maternal relatives of the subject and exhibited variable heteroplasmy. Our current observation, together with a recent report for a benign 154-bp deletion in the mtDNA control region, suggests that the control of mtDNA replication may be more complex than we had thought. (c) 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20151402     DOI: 10.1002/humu.21220

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  16 in total

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Review 3.  Physiology and pathophysiology of mitochondrial DNA.

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7.  Mitochondrial DNA copy number, but not haplogroup, confers a genetic susceptibility to leprosy in Han Chinese from Southwest China.

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8.  Somatic mtDNA mutation spectra in the aging human putamen.

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9.  Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy.

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10.  Leukocyte mitochondrial DNA copy number in blood is not associated with major depressive disorder in young adults.

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