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Effects of age on segregation of the X and Y chromosomes in cultured lymphocytes from Chinese men

Effects of age on segregation of the X and Y chromosomes in cultured lymphocytes from Chinese men
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摘要 Chromosome malsegregation in binucleated lymphocytes is a useful endpoint to evaluate age effect on genetic stability. However, the investigations on chromosome malsegregation in binucleated lymphocytes from Chinese are scarce. In this study, peripheral blood lym- phocytes were collected from 14 old (60-70 years) and 10 young (22-26 years) healthy Chinese men. To detect malsegregation of the sex chromosomes, multi-color fluorescence in situ hybridization (FISH) was performed on binucleated lymphocytes, cytokinesis-blocked by cytochalasin B at the first mitosis after phytohaemagglutinin stimulation. Compared with that in young men, a significant increase in frequencies of loss of chromosome X (9.2± 3.2‰ vs. 1.1 ± 0.9‰, P 〈 0.001) and Y (2.5 ± 1.9‰ vs. 0.2± 0.3‰, P 〈 0.001) was found in old men. Similarly, nondisjunction of chromosome X (16.5± 3.4‰ vs. 3.5 ± 1.1‰, P 〈 0.001) and Y (7.2 ± 2.6‰ vs. 2.4 ± 1.3‰, P 〈 0.001) occurred more frequently in old men than in young men. Regardless of donor's age, nondisjunction is more prevalent than loss for both chromosome X and Y. The frequencies of observed simultaneous malsegregation were relatively higher than the expected, suggest- ing an association between malsegregation. These results indicated that in Chinese men, malsegregation of the sex chromosomes increases with age in an associated fashion, and nondisjunction accounts for the majority of spontaneous chromosome malsegregation. Chromosome malsegregation in binucleated lymphocytes is a useful endpoint to evaluate age effect on genetic stability. However, the investigations on chromosome malsegregation in binucleated lymphocytes from Chinese are scarce. In this study, peripheral blood lym- phocytes were collected from 14 old (60-70 years) and 10 young (22-26 years) healthy Chinese men. To detect malsegregation of the sex chromosomes, multi-color fluorescence in situ hybridization (FISH) was performed on binucleated lymphocytes, cytokinesis-blocked by cytochalasin B at the first mitosis after phytohaemagglutinin stimulation. Compared with that in young men, a significant increase in frequencies of loss of chromosome X (9.2± 3.2‰ vs. 1.1 ± 0.9‰, P 〈 0.001) and Y (2.5 ± 1.9‰ vs. 0.2± 0.3‰, P 〈 0.001) was found in old men. Similarly, nondisjunction of chromosome X (16.5± 3.4‰ vs. 3.5 ± 1.1‰, P 〈 0.001) and Y (7.2 ± 2.6‰ vs. 2.4 ± 1.3‰, P 〈 0.001) occurred more frequently in old men than in young men. Regardless of donor's age, nondisjunction is more prevalent than loss for both chromosome X and Y. The frequencies of observed simultaneous malsegregation were relatively higher than the expected, suggest- ing an association between malsegregation. These results indicated that in Chinese men, malsegregation of the sex chromosomes increases with age in an associated fashion, and nondisjunction accounts for the majority of spontaneous chromosome malsegregation.
出处 《Journal of Genetics and Genomics》 SCIE CAS CSCD 2009年第8期467-474,共8页 遗传学报(英文版)
基金 supported by the National Natural Science Foundation of China (No.30571030,30671168 and 30725013) the Program of "One Hundred Talented People" (No.KJ207004) of the Chinese Academy of Sciences
关键词 chromosome loss NONDISJUNCTION chromosome X chromosome Y LYMPHOCYTE Chinese men chromosome loss nondisjunction chromosome X chromosome Y lymphocyte Chinese men
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参考文献39

  • 1Baker, D.J., Jeganathan, K.B., Cameron, J.D., Thompson, M., Juneja, S., Kopecka, A., Kumar, R., Jenkins, R.B., de Groen, P.C., Roche, P., and van Deursen, J.M. (2004). BubR1 insufficiency causes early onset of aging-associated phenotypes and infertility in mice. Nat. Genet. 36: 744-749.
  • 2Bakou, K., Stephanou, G., Andrianopoulos, C., and Demopoulos, N.A. (2002). Spontaneous and spindle poison-induced micronuclei and chromosome non-disjunction in cytokinesis-blocked lymphocytes from two age groups of women. Mutagenesis 17: 233-239.
  • 3Boffetta, P., van der Hel, O., Norppa, H., Fabianova, E., Fucic, A., Gundy, S., Lazutka, J., Cebulska-Wasilewska, A., Puskailerova, D., Znaor, A., Kelecsenyi, Z., Kurtinaitis, J., Rachtan, J., Forni, A., Vermeulen, R., and Bonassi, S. (2007). Chromosomal aberrations and cancer risk: Results of a cohort study from Central Europe. Am. J. Epidemiol. 165: 36-43.
  • 4Bonassi, S., Znaor, A., Ceppi, M., Lando, C., Chang, W.P., Holland, N., Kirsch-Volders, M., Zeiger, E., Ban, S., Barale, R., Bigatti, M.P., Bolognesi, C., Cebulska-Wasilewska, A., Fabianova, E., Fucic, A., Hagmar, L., Joksic, G., Martelli, A., Migliore, L., Mirkova, E., Scarfi, M.R., Zijno, A., Norppa, H., and Fenech, M. (2007). An increased micronucleus frequency in peripheral blood lymphocytes predicts the risk of cancer in humans. Carcinogenesis 28: 625-631.
  • 5Carere, A., Antoccia, A., Cimini, D., Crebelli, R., Degrassi, F., Leopardi, P., Marcon, F., Sgura, A., Tanzarella, C., and Zijno, A. (1999). Analysis of chromosome loss and non-disjunction in cytokinesis-blocked lymphocytes of 24 male subjects. Mutagenesis 14: 491-496.
  • 6Catalan, J., Autio, K., Kuosma, E., and Norppa, H. (1998). Age-dependent inclusion of sex chromosomes in lymphocyte micronuclei of man. Am. J. Hum. Genet. 63: 1464-1472.
  • 7Catalan, J., Surralles, J., Falck, G.C., Autio, K., and Norppa, H. (2000). Segregation of sex chromosomes in human lymphocytes. Mutagenesis 15: 251-255.
  • 8Cimini, D., and Degrassi, F. (2005). Aneuploidy: A matter of bad connections. Trends Cell Biol. 15: 442-451.
  • 9Cleveland, D.W., Mao, Y., and Sullivan, K.F. (2003). Centromeres and kinetochores: From epigenetics to mitotic checkpoint signaling. Cell 112: 407-421.
  • 10Fenech, M., and Morley, A.A. (1989). Kinetochore detection in micronuclei: An alternative method for measuring chromosome loss. Mutagenesis 4: 98-104.

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