Age-Related Somatic Structural Changes in the Nuclear Genome of Human Blood Cells

详细信息    查看全文

• 作者：Lars  ; A. Forsberg¹ ; Chiara Rasi¹ ; Hamid  ; R. Razzaghian¹ ; Geeta Pakalapati¹ ; Lindsay Waite² ; Krista  ; Stanton Thilbeault² ; Anna Ronowicz³ ; Nathan  ; E. Wineinger⁴ ; Hemant  ; K. Tiwari⁴ ; Dorret Boomsma⁵ ; Maxwell  ; P. Westerman⁶ ; Jennifer  ; R. Harris⁷ ; Robert Lyle⁸ ; Magnus Essand¹ ; Fredrik Eriksson¹ ; Themistocles  ; L. Assimes⁹ ; Carlos Iribarren¹⁰ ; Eric Strachan¹¹ ; Terrance  ; P. O'Hanlon¹² ; Lisa  ; G. Rider¹² ; Frederick  ; W. Miller¹² ; Vilmantas Giedraitis¹³ ; Lars Lannfelt¹³ ; Martin Ingelsson¹³ ; Arkadiusz Piotrowski³ ; Nancy  ; L. Pedersen¹⁴ ; Devin Absher² ; Jan  ; P. Dumanski¹ ; ^{jan.dumanski@igp.uu.se}
• 刊名：The American Journal of Human Genetics
• 出版年：2012
• 出版时间：10 February 2012
• 年：2012
• 卷：90
• 期：2
• 页码：217-228
• 全文大小：2039 K

文摘

Structural variations are among the most frequent interindividual genetic differences in the human genome. The frequency and distribution of de novo somatic structural variants in normal cells is, however, poorly explored. Using age-stratified cohorts of 318 monozygotic (MZ) twins and 296 single-born subjects, we describe age-related accumulation of copy-number variation in the nuclear genomes in?vivo and frequency changes for both megabase- and kilobase-range variants. Megabase-range aberrations were found in 3.4 % (9 of 264) of subjects ?0 years old; these subjects included 78 MZ twin pairs and 108 single-born individuals. No such findings were observed in 81 MZ pairs or 180 single-born subjects who were ?5 years old. Recurrent region- and gene-specific mutations, mostly deletions, were observed. Longitudinal analyses of 43 subjects whose data were collected 7?9 years apart suggest considerable variation in the rate of accumulation of clones carrying structural changes. Furthermore, the longitudinal analysis of individuals with structural aberrations suggests that there is a natural self-removal of aberrant cell clones from peripheral blood. In three healthy subjects, we detected somatic aberrations characteristic of patients with myelodysplastic syndrome. The recurrent rearrangements uncovered here are candidates for common age-related defects in human blood cells. We anticipate that extension of these results will allow determination of the genetic age of different somatic-cell lineages and estimation of possible individual differences between genetic and chronological age. Our work might also help to explain the cause of an age-related reduction in the number of cell clones in the blood; such a reduction is one of the hallmarks of immunosenescence.