GENETIC-ANALYSIS OF INDEFINITE DIVISION IN HUMAN-CELLS - EVIDENCE FOR A CELL SENESCENCE-RELATED GENE(S) ON HUMAN CHROMOSOME-4

被引:212
作者
NING, Y
WEBER, JL
KILLARY, AM
LEDBETTER, DH
SMITH, JR
PEREIRASMITH, OM
机构
[1] UNIV TEXAS, MD ANDERSON CANC CTR, DIV LAB MED, HOUSTON, TX 77030 USA
[2] MARSHFIELD MED RES FDN, MARSHFIELD, WI 54449 USA
[3] BAYLOR UNIV, INST MOLEC GENET,DEPT CELL BIOL,DEPT MED, DIV MOLEC VIROL, HOUSTON, TX 77030 USA
关键词
MICROCELL HYBRIDS; CELL PROLIFERATION; CELL IMMORTALIZATION; AGING;
D O I
10.1073/pnas.88.13.5635
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
Earlier studies had demonstrated that fusion of normal with immortal human cells yielded hybrids having limited division potential. This indicated that the phenotype of limited proliferation (cellular senescence) is dominant and that immortal cells result from recessive changes in normal growth-regulatory genes. In additional studies, we exploited the fact that the immortal phenotype is recessive and, by fusing various immortal human cell lines with each other, identified four complementation groups for indefinite division. Assignment of cell lines to specific groups allowed us to take a focused approach to identify the chromosomes and genes involved in growth regulation that have been modified in immortal cells. We report here that introduction of a normal human chromosome 4 into three immortal cell lines (HeLa, J82, T98G) assigned to complementation group B resulted in loss of proliferation and reversal of the immortal phenotype. No effect on the proliferation potential of cell lines representative of the other complementation groups was observed. This result suggests that a gene(s) involved in cellular senescence and normal growth regulation resides on chromosome 4.
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页码:5635 / 5639
页数:5
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