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The role of the Bub1 gene in chromosomal instability and cancer progression.

机译:Bub1基因在染色体不稳定和癌症进展中的作用。

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摘要

Colorectal cancer (CRC) is an important cause of mortality and morbidity in the world. Some CRC tumors show chromosomal instability (CIN) and others show microsatellite instability. The cause for microsatellite instability is considered to be the result of mutations in DNA mismatch repair genes but the genetic basis for CIN is not well understood. We hypothesized that CIN might result from mutations in genes involved in the mitotic checkpoint.; Bub1 is a gene involved in mitotic checkpoint. Mutations in Bub1 have been identified in CRC tumors. To examine the role of Bub1 in cancer and chromosomal instability, we generated mice that carry a null mutation in the Bub1 gene.; Our data shows that Bub1 is necessary for embryogenesis because homozygous Bub1 mutant mice do not survive beyond 3.5 days of development. The generation of Bub1 double targeted ES cells demonstrated that inactivation of the gene does not lead to cell lethality.; Chromosome segregation was examined in Bub1+/− and wild-type (WT) cell lines. At different passages the Bub1+/− line showed a higher percentage of aneuploid cells. To confirm this observation FISH analysis was performed in blood cells of WT and Bub1+/− mice using probes for chromosomes 9 and 17. Modest chromosomal instability was observed in the Bub1+/− samples.; Bub1+/− mice are fertile and susceptible to develop tumors late in their lives. Bub1+/− mice were bred to Apc1638N and Msh2 mutant mice. There was no difference in the incidence or multiplicity of tumors suggesting that genomic instability provided by Bub1 heterozygosity is insufficient to significantly affect the biology of the tumors in these double mutants. The tumors were analyzed by microarray-based Comparative Genomic Hybridization (aCGH) and no difference was observed in the genomic changes of the tumors in the presence or absence of the Bub1+/− mutation. The results showed clear evidence of the role of Msh2 in the regulation of homeologous recombination.; Taken together, these results suggest that the Bub1 gene is essential for normal survival. Bub1 heterozygosity leads to a mild chromosomal instability phenotype. This degree of chromosomal instability does not significantly affect the phenotype of Apc 1638N and Msh2−/− mutant mice.
机译:大肠癌(CRC)是世界上死亡率和发病率的重要原因。一些CRC肿瘤显示染色体不稳定(CIN),而另一些则显示微卫星不稳定。微卫星不稳定性的原因被认为是DNA错配修复基因突变的结果,但CIN的遗传基础尚不十分清楚。我们假设CIN可能是由有丝分裂检查点相关基因的突变引起的。 Bub1 是一个参与有丝分裂检查点的基因。在CRC肿瘤中已经鉴定出 Bub1 的突变。为了检测 Bub1 在癌症和染色体不稳定中的作用,我们产生了在 Bub1 基因中带有无效突变的小鼠。我们的数据表明, Bub1 对于胚胎发生是必需的,因为纯合的 Bub1 突变小鼠不能存活超过3.5天。 Bub1 双重靶向ES细胞的产生证明该基因的失活不会导致细胞致死。在 Bub1 + /-/ super细胞和野生型(WT)细胞系中检查染色体分离。在不同的传代中, Bub1 +/- 系显示出更高比例的非整倍体细胞。为了证实这一观察结果,使用9号和17号染色​​体探针在WT和 Bub1 +/- 小鼠的血细胞中进行了FISH分析,观察到在中存在适度的染色体不稳定> Bub1 +/− 样本。 Bub1 +/- 小鼠具有繁殖力,并且很容易在生命的晚期发展成肿瘤。将 Bub1 +/- 小鼠繁殖到 Apc 1638N Msh2 突变小鼠。肿瘤的发生率或多样性没有差异,表明 Bub1 杂合性提供的基因组不稳定性不足以显着影响这些双重突变体中的肿瘤生物学。通过基于微阵列的比较基因组杂交(aCGH)分析肿瘤,在存在或不存在 Bub1 +/- 突变。结果清楚表明 Msh2 在同源重组调控中的作用。综上所述,这些结果表明 Bub1 基因对于正常生存至关重要。 Bub1 杂合性导致轻度的染色体不稳定表型。这种程度的染色体不稳定性不会显着影响 Apc 1638N Msh2 -/-突变小鼠的表型。

著录项

  • 作者

    Carrion, Danaise V.;

  • 作者单位

    Yeshiva University.;

  • 授予单位 Yeshiva University.;
  • 学科 Biology Genetics.; Biology Molecular.; Health Sciences Oncology.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 257 p.
  • 总页数 257
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 遗传学;分子遗传学;肿瘤学;
  • 关键词

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