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Free-living human cells reconfigure their chromosomes in the evolution back to uni-cellularity.
Xu, Jin; Peng, Xinxin; Chen, Yuxin; Zhang, Yuezheng; Ma, Qin; Liang, Liang; Carter, Ava C; Lu, Xuemei; Wu, Chung-I.
Affiliation
  • Xu J; Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.
  • Peng X; Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.
  • Chen Y; State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-Sen University, Guangzhou, China.
  • Zhang Y; Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.
  • Ma Q; Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.
  • Liang L; University of Chinese Academy of Sciences, Beijing, China.
  • Carter AC; Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.
  • Lu X; University of Chinese Academy of Sciences, Beijing, China.
  • Wu CI; Center for Personal Dynamic Regulomes, Stanford University School of Medicine, Stanford, United States.
Elife ; 62017 12 18.
Article in En | MEDLINE | ID: mdl-29251591
ABSTRACT
Cells of multi-cellular organisms evolve toward uni-cellularity in the form of cancer and, if humans intervene, continue to evolve in cell culture. During this process, gene dosage relationships may evolve in novel ways to cope with the new environment and may regress back to the ancestral uni-cellular state. In this context, the evolution of sex chromosomes vis-a-vis autosomes is of particular interest. Here, we report the chromosomal evolution in ~ 600 cancer cell lines. Many of them jettisoned either Y or the inactive X; thus, free-living male and female cells converge by becoming 'de-sexualized'. Surprisingly, the active X often doubled, accompanied by the addition of one haploid complement of autosomes, leading to an XA ratio of 23 from the extant ratio of 12. Theoretical modeling of the frequency distribution of XA karyotypes suggests that the 23 ratio confers a higher fitness and may reflect aspects of sex chromosome evolution.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sex Chromosomes / Adaptation, Biological / Chromosomes, Human / Cell Proliferation Limits: Humans Language: En Journal: Elife Year: 2017 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sex Chromosomes / Adaptation, Biological / Chromosomes, Human / Cell Proliferation Limits: Humans Language: En Journal: Elife Year: 2017 Type: Article Affiliation country: China