Chromosome nondisjunction yields tetraploid rather than aneuploid cells in human cell lines

被引:332
作者
Shi, QH [1 ]
King, RW [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
关键词
D O I
10.1038/nature03958
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although mutations in cell cycle regulators or spindle proteins can perturb chromosome segregation(1-7), the causes and consequences of spontaneous mitotic chromosome nondisjunction in human cells are not well understood. It has been assumed that nondisjunction of a chromosome during mitosis will yield two aneuploid daughter cells. Here we show that chromosome nondisjunction is tightly coupled to regulation of cytokinesis in human cell lines, such that nondisjunction results in the formation of tetraploid rather than aneuploid cells. We observed that spontaneously arising binucleated cells exhibited chromosome mis-segregation rates up to 166-fold higher than the overall mitotic population. Long-term imaging experiments indicated that most binucleated cells arose through a bipolar mitosis followed by regression of the cleavage furrow hours later. Nondisjunction occurred with high frequency in cells that became binucleated by furrow regression, but not in cells that completed cytokinesis to form two mononucleated cells. Our findings indicate that nondisjunction does not directly yield aneuploid cells, but rather tetraploid cells that may subsequently become aneuploid through further division. The coupling of spontaneous segregation errors to furrow regression provides a potential explanation for the prevalence of hyperdiploid chromosome number and centrosome amplification observed in many cancers(8,9).
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页码:1038 / 1042
页数:5
相关论文
共 31 条
[11]   Mutations in the APC tumour suppressor gene cause chromosomal instability [J].
Fodde, R ;
Kuipers, J ;
Rosenberg, C ;
Smits, R ;
Kielman, M ;
Gaspar, C ;
van Es, JH ;
Bruekel, C ;
Wiegant, J ;
Giles, RH ;
Clevers, H .
NATURE CELL BIOLOGY, 2001, 3 (04) :433-438
[12]   17p (p53) allelic losses, 4N (G(2)/tetraploid) populations, and progression to aneuploidy in Barrett's esophagus [J].
Galipeau, PC ;
Cowan, DS ;
Sanchez, CA ;
Barrett, MT ;
Emond, MJ ;
Levine, DS ;
Rabinovitch, PS ;
Reid, BJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :7081-7084
[13]   Rb inactivation promotes genomic instability by uncoupling cell cycle progression from mitotic control [J].
Hernando, E ;
Nahlé, Z ;
Juan, G ;
Diaz-Rodriguez, E ;
Alaminos, M ;
Hemann, M ;
Michel, L ;
Mittal, V ;
Gerald, W ;
Benezra, R ;
Lowe, SW ;
Cordon-Cardo, C .
NATURE, 2004, 430 (7001) :797-802
[14]   Securin is required for chromosomal stability in human cells [J].
Jallepalli, PV ;
Waizenegger, IC ;
Bunz, F ;
Langer, S ;
Speicher, MR ;
Peters, JM ;
Kinzler, KW ;
Vogelstein, B ;
Lengauer, C .
CELL, 2001, 105 (04) :445-457
[15]   Histone-GFP fusion protein enables sensitive analysis of chromosome dynamics in living mammalian cells [J].
Kanda, T ;
Sullivan, KF ;
Wahl, GM .
CURRENT BIOLOGY, 1998, 8 (07) :377-385
[16]  
Kaneko Y, 2000, GENE CHROMOSOME CANC, V29, P89, DOI 10.1002/1098-2264(2000)9999:9999<::AID-GCC1021>3.0.CO
[17]  
2-Y
[18]   A role for the Adenomatous Polyposis Coli protein in chromosome segregation [J].
Kaplan, KB ;
Burds, AA ;
Swedlow, JR ;
Bekir, SS ;
Sorger, PK ;
Näthke, IS .
NATURE CELL BIOLOGY, 2001, 3 (04) :429-432
[19]   Lethality to human cancer cells through massive chromosome loss by inhibition of the mitotic checkpoint [J].
Kops, GJPL ;
Foltz, DR ;
Cleveland, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (23) :8699-8704
[20]  
Macville M, 1999, CANCER RES, V59, P141