Fagarasanu Monica, Fagarasanu Andrei, Rachubinski Richard A
Department of Cell Biology, University of Alberta, Medical Sciences Building 5-14, Edmonton, Alberta, Canada T6G 2H7.
Biochim Biophys Acta. 2006 Dec;1763(12):1669-77. doi: 10.1016/j.bbamcr.2006.08.015. Epub 2006 Aug 22.
Eukaryotic cells have evolved molecular mechanisms to ensure the faithful partitioning of cellular components during cell division. The budding yeast Saccharomyces cerevisiae has to actively deliver about half of its organelles to the growing bud, while retaining the remaining organelles in the mother cell. Until lately, little was known about the inheritance of peroxisomes. Recent studies have identified the peroxisomal proteins Inp1p and Inp2p as two key regulators of peroxisome inheritance that perform antagonistic functions. Inp1p is required for the retention of peroxisomes in mother cells, whereas Inp2p promotes the bud-directed movement of these organelles. Inp1p anchors peroxisomes to the cell cortex by interacting with specific structures lining the cell periphery. On the other hand, Inp2p functions as the peroxisome-specific receptor for the class V myosin, Myo2p, thereby linking peroxisomes to the translocation machinery that propels peroxisome movement. Tight coordination between Inp1p and Inp2p ensures a fair and harmonious spatial segregation of peroxisomes upon cell division.
真核细胞已经进化出分子机制,以确保细胞分裂过程中细胞成分的准确分配。出芽酵母酿酒酵母必须将大约一半的细胞器主动运输到生长中的芽中,同时将其余的细胞器保留在母细胞中。直到最近,人们对过氧化物酶体的遗传了解甚少。最近的研究已经确定过氧化物酶体蛋白Inp1p和Inp2p是过氧化物酶体遗传的两个关键调节因子,它们发挥着拮抗作用。Inp1p是过氧化物酶体保留在母细胞中所必需的,而Inp2p则促进这些细胞器向芽的定向移动。Inp1p通过与细胞周边的特定结构相互作用,将过氧化物酶体锚定在细胞皮层。另一方面,Inp2p作为V类肌球蛋白Myo2p的过氧化物酶体特异性受体,从而将过氧化物酶体与推动过氧化物酶体移动的转运机制联系起来。Inp1p和Inp2p之间的紧密协调确保了细胞分裂时过氧化物酶体的公平和和谐的空间分离。