|
|
Blood, 15 January 2004, Vol. 103, No. 2, pp. 553-561.
Prepublished online as a Blood First Edition Paper on September 22, 2003; DOI 10.1182/blood-2003-05-1724.
Previous Article | Table of Contents | Next Article 
HEMATOPOIESIS
Marked mitochondrial DNA sequence heterogeneity in single CD34+ cell clones from normal adult bone marrow
Myung Geun Shin,
Sachiko Kajigaya,
J. Philip McCoy, Jr,
Barbara C. Levin, and
Neal S. Young
From the Hematology Branch, Flow Cytometry Core Facility, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD; and Biotechnology Division, Chemical Science and Technology Laboratory, National Institute of Standards and Technology, Gaithersburg, MD.
Somatic mitochondrial DNA (mtDNA) mutations accumulate with age in postmitotic tissues but have been postulated to be diluted and lost in continually proliferating tissues such as bone marrow (BM). Having observed marked sequence variation among healthy adult individuals' total BM cell mtDNA, we undertook analysis of the mtDNA control region in a total of 611 individual CD34+ clones from 6 adult BM donors and comparison of these results with the sequences from 580 CD34+ clones from 5 umbilical cord blood (CB) samples. On average, 25% (range, 11% to 50%) of individual CD34+ clones from adult BM showed mtDNA heterogeneity, or sequence differences from the aggregate mtDNA sequence of total BM cells of the same individual. In contrast, only 1.6% of single CD34+ clones from CB showed mtDNA sequence variation from the aggregate pattern. Thus, age-dependent accumulation of mtDNA mutations appears relatively common in a mitotically active human tissue and may provide a method to approximate the mutation rate in mammalian cells, to assess the contribution of reactive oxygen species to genomic instability, and for natural "marking" of hematopoietic stem cells; our data also have important implications for the aging process, forensic identifications, and anthropologic conclusions dependent on the mtDNA sequence.

CiteULike Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
Y.-G. Yao, R. W. Childs, S. Kajigaya, J. P. McCoy Jr., and N. S. Young
Mitochondrial DNA Sequence Heterogeneity of Single CD34+ Cells After Nonmyeloablative Allogeneic Stem Cell Transplantation
Stem Cells,
October 1, 2007;
25(10):
2670 - 2676.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H.-W. Park, Y. Ahn, M.-H. Jeong, J.-G. Cho, J.-C. Park, J.-C. Kang, M.-G. Shin, J.-H. Shin, S.-P. Suh, D.-W. Ryang, et al.
Chronic atrial fibrillation associated with somatic mitochondrial DNA mutations in human atrial tissue
J. Clin. Pathol.,
August 1, 2007;
60(8):
948 - 950.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Lee, M.-G. Shin, W.-H. Jo, M.-J. Kim, H.-R. Kim, W.-S. Lee, D.-H. Park, J.-H. Won, J.-H. Shin, S.-P. Suh, et al.
Association between Helicobacter pylori-Related Peptic Ulcer Tissue and Somatic Mitochondrial DNA Mutations
Clin. Chem.,
July 1, 2007;
53(7):
1390 - 1392.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y.-G. Yao, F. M. Ellison, J. P. McCoy, J. Chen, and N. S. Young
Age-dependent accumulation of mtDNA mutations in murine hematopoietic stem cells is modulated by the nuclear genetic background
Hum. Mol. Genet.,
February 1, 2007;
16(3):
286 - 294.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y.-G. Yao, Y. Ogasawara, S. Kajigaya, J. J. Molldrem, R. P. Falcao, M.-C. Pintao, J. P. McCoy Jr, E. G. Rizzatti, and N. S. Young
Mitochondrial DNA sequence variation in single cells from leukemia patients
Blood,
January 15, 2007;
109(2):
756 - 762.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H-J Bandelt, Q-P Kong, W Parson, and A Salas
More evidence for non-maternal inheritance of mitochondrial DNA?
J. Med. Genet.,
December 1, 2005;
42(12):
957 - 960.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Ogasawara, K. Nakayama, M. Tarnowka, J. P. McCoy Jr, S. Kajigaya, B. C. Levin, and N. S. Young
Mitochondrial DNA spectra of single human CD34+ cells, T cells, B cells, and granulocytes
Blood,
November 1, 2005;
106(9):
3271 - 3284.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. G. Shin, S. Kajigaya, M. Tarnowka, J. P. McCoy Jr, B. C. Levin, and N. S. Young
Mitochondrial DNA sequence heterogeneity in circulating normal human CD34 cells and granulocytes
Blood,
June 15, 2004;
103(12):
4466 - 4477.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|