Suh Mi Ra, Han Ji Woong, No Yi Ran, Lee JooHun
Department of Biology and Institute of Bioscience and Biotechnology, Yonsei University, Seoul 120-749, Korea.
Cell Motil Cytoskeleton. 2002 Jun;52(2):66-81. doi: 10.1002/cm.10033.
The distribution of two proteins in Naegleria gruberi, N-gammaTRP (Naegleria gamma-tubulin-related protein) and N-PRP (Naegleria pericentrin-related protein), was examined during the de novo formation of basal bodies and flagella that occurs during the differentiation of N. gruberi. After the initiation of differentiation, N-gammaTRP and N-PRP began to concentrate at the same site within cells. The percentage of cells with a concentrated region of N-gammaTRP and N-PRP was maximal (68%) at 40 min when the synthesis of tubulin had just started but no assembled microtubules were visible. When concentrated tubulin became visible (60 min), the region of concentrated N-gammaTRP and N-PRP was co-localized with the tubulin spot and then flagella began to elongate from the region of concentrated tubulin. When cells had elongated flagella, the concentrated N-gammaTRP and N-PRP were translocated to the opposite end of the flagellated cells and disappeared. The transient concentration of N-gammaTRP coincided with the transient formation of an F-actin spot at which N-gammaTRP and alpha-tubulin mRNA were co-localized. The concentration of N-gammaTRP and formation of the F-actin spot occurred without the formation of microtubules but were inhibited by cytochalasin D. These observations suggest that the regional concentration of N-gammaTRP and N-PRP is mediated by actin filaments and might provide a site of microtubule nucleation for the assembly of newly synthesized tubulins into basal bodies and flagella.
研究了两种蛋白质,即格氏耐格里阿米巴(Naegleria gruberi)中的N-γTRP(格氏耐格里阿米巴γ-微管蛋白相关蛋白)和N-PRP(格氏耐格里阿米巴中心粒外周蛋白相关蛋白)在格氏耐格里阿米巴分化过程中从头形成基体和鞭毛期间的分布情况。分化开始后,N-γTRP和N-PRP开始在细胞内的同一位置聚集。当微管蛋白的合成刚刚开始但尚未可见组装的微管时,在40分钟时N-γTRP和N-PRP聚集区域的细胞百分比达到最大值(68%)。当可见聚集的微管蛋白时(60分钟),N-γTRP和N-PRP的聚集区域与微管蛋白斑点共定位,然后鞭毛开始从聚集的微管蛋白区域伸长。当细胞有伸长的鞭毛时,聚集的N-γTRP和N-PRP转移到有鞭毛细胞的另一端并消失。N-γTRP的瞬时聚集与F-肌动蛋白斑点的瞬时形成同时发生,N-γTRP和α-微管蛋白mRNA在该斑点处共定位。N-γTRP的聚集和F-肌动蛋白斑点的形成在没有微管形成的情况下发生,但被细胞松弛素D抑制。这些观察结果表明,N-γTRP和N-PRP的区域聚集是由肌动蛋白丝介导的,并且可能为将新合成的微管蛋白组装成基体和鞭毛提供微管成核位点。