首页> 外文期刊>Molecular biology of the cell >Coupling of posterior cytoskeletal morphogenesis to the G1/S transition in the Trypanosoma brucei cell cycle
【24h】

Coupling of posterior cytoskeletal morphogenesis to the G1/S transition in the Trypanosoma brucei cell cycle

机译:后布鲁氏锥虫细胞周期中细胞骨架形态发生与G1 / S过渡的耦合

获取原文
获取原文并翻译 | 示例
           

摘要

The expression levels of four Cdc2-related kinases (CRK1, 2, 4, and 6) in the procyclic form of Trypanosoma brucei were knocked down in pairs using the RNA interference (RNAi) technique. A double knockdown of CRK1 and CRK2 resulted in arrested cell growth in the G1 phase accompanied by an apparent cessation of nuclear DNA synthesis. The arrested cells became elongated at the posterior end like the G1-phase cells generated by knockdown of CycE1/CYC2 in a previous study. However, similar to5% of the G1 cells in the current study also possessed multiply branched posterior ends, which have not previously been observed in T. brucei. DAPI and immunofluorescence staining showed a single nucleus, kinetoplast, basal body, and flagellum in the anterior portion of each G1 cell. The split and grossly extended posterior ends were heavily stained with antibodies to tyrosinated alpha-tubulin, suggesting an accumulation of newly synthesized microtubules. A significant population of anucleate cells (zoids), apparently derived from kinetoplast-dictated cytokinesis and cell division of the G1 cells, also had extended and branched posterior ends filled with newly synthesized microtubules. This continued posterior extension of microtubules in the G1 cells and zoids suggests that CRK1 and CRK2 exert a coordinated control on G1/S passage and the limited growth of the microtubule corset toward the posterior end. This connection may provide a new insight into the mechanism of morphological maintenance of an ancient protist during its cell cycle progression.
机译:使用RNA干扰(RNAi)技术成对地降低了布鲁氏锥虫的前环形式的四种Cdc2相关激酶(CRK1、2、4和6)的表达水平。 CRK1和CRK2的双重击倒导致G1期细胞生长停滞,并伴随着核DNA合成的明显停止。被捕的细胞在后端变得拉长,就像先前研究中通过敲除CycE1 / CYC2产生的G1期细胞一样。但是,当前研究中约有5%的G1细胞也具有多分支的后端,这在布鲁氏菌中未曾观察到。 DAPI和免疫荧光染色在每个G1细胞的前部显示单个核,运动塑料,基体和鞭毛。分裂的和明显延长的后端被酪氨酸α-微管蛋白抗体严重染色,表明新合成的微管积聚。明显地由动质体决定的胞质分裂和G1细胞的细胞分裂衍生的大量无核细胞(类固醇)也具有延伸和分支的后端,充满了新合成的微管。 G1细胞和Zoids中微管的这种持续向后延伸表明,CRK1和CRK2对G1 / S通道和微管紧身胸衣向后端的有限生长施加了协调控制。这种联系可以为古代生物在细胞周期进程中的形态维持机制提供新的见解。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号