Webster D R, Gundersen G G, Bulinski J C, Borisy G G
J Cell Biol. 1987 Jul;105(1):265-76. doi: 10.1083/jcb.105.1.265.
Detyrosinated (Glu) tubulin was prepared from porcine brain and microinjected into human fibroblasts and Chinese hamster ovary (CHO) cells. Glu tubulin assembled onto the ends of preexisting microtubules and directly from the centrosome within minutes of its microinjection. Incorporation into the cytoskeleton continued until almost all of the microtubules were copolymers of Glu and tyrosinated (Tyr) tubulin. However, further incubation resulted in the progressive and ultimately complete loss of Glu-staining microtubules. Glu tubulin injected into nocodazole-treated cells was converted to Tyr tubulin by a putative tubulin/tyrosine ligase activity. The observed decrease in staining with the Glu antibody over time was used to analyze microtubule turnover in microinjected cells. The mode of Glu disappearance was analyzed quantitatively by tabulating the number of Glu-Tyr copolymers and Tyr-only microtubules at fixed times after injection. The proportion of Glu-Tyr copolymers decreased progressively over time and no segmentally labeled microtubules were observed, indicating that microtubules turn over rapidly and individually. Our results are consistent with a closely regulated tyrosination-detyrosination cycle in living cells and suggest that microtubule turnover is mediated by dynamic instability.
去酪氨酸化(Glu)微管蛋白是从猪脑中制备的,并显微注射到人类成纤维细胞和中国仓鼠卵巢(CHO)细胞中。Glu微管蛋白在显微注射后的几分钟内组装到预先存在的微管末端,并直接从中心体组装。整合到细胞骨架中的过程持续进行,直到几乎所有微管都是Glu和酪氨酸化(Tyr)微管蛋白的共聚物。然而,进一步孵育导致Glu染色的微管逐渐并最终完全消失。注射到诺考达唑处理细胞中的Glu微管蛋白通过一种假定的微管蛋白/酪氨酸连接酶活性转化为Tyr微管蛋白。随着时间的推移,观察到的Glu抗体染色减少被用于分析显微注射细胞中的微管周转。通过在注射后固定时间统计Glu-Tyr共聚物和仅含Tyr的微管数量,对Glu消失的模式进行了定量分析。Glu-Tyr共聚物的比例随时间逐渐降低,未观察到分段标记的微管,这表明微管快速且独立地周转。我们的结果与活细胞中严格调控的酪氨酸化-去酪氨酸化循环一致,并表明微管周转是由动态不稳定性介导的。