Bowman Barry J, Draskovic Marija, Freitag Michael, Bowman Emma Jean
Department of Molecular, Cell, and Developmental Biology, University of California, Santa Cruz, CA 95064, USA.
Eukaryot Cell. 2009 Dec;8(12):1845-55. doi: 10.1128/EC.00174-09. Epub 2009 Oct 2.
We wanted to examine the cellular locations of four Neurospora crassa proteins that transport calcium. However, the structure and distribution of organelles in live hyphae of N. crassa have not been comprehensively described. Therefore, we made recombinant genes that generate translational fusions of putative organellar marker proteins with green or red fluorescent protein. We observed putative endoplasmic reticulum proteins, encoded by grp-78 and dpm, in the nuclear envelope and associated membranes. Proteins of the vacuolar membrane, encoded by vam-3 and vma-1, were in an interconnected network of small tubules and vesicles near the hyphal tip, while in more distal regions they were in large and small spherical vacuoles. Mitochondria, visualized with tagged ARG-4, were abundant in all regions of the hyphae. Similarly, we tagged the four N. crassa proteins that transport calcium with green or red fluorescent protein to examine their cellular locations. NCA-1 protein, a homolog of the SERCA-type Ca(2+)-ATPase of animal cells, colocalized with the endoplasmic reticulum markers. The NCA-2 and NCA-3 proteins are homologs of Ca(2+)-ATPases in the vacuolar membrane in yeast or in the plasma membrane in animal cells. They colocalized with markers in the vacuolar membrane, and they also occurred in the plasma membrane in regions of the hyphae more than 1 mm from the tip. The cax gene encodes a Ca(2+)/H(+) exchange protein found in vacuoles. As expected, the CAX protein localized to the vacuolar compartment. We observed, approximately 50 to 100 mum from the tip, a few spherical organelles that had high amounts of tagged CAX protein and tagged subunits of the vacuolar ATPase (VMA-1 and VMA-5). We suggest that this organelle, not described previously in N. crassa, may have a role in sequestering calcium.
我们想要研究粗糙脉孢菌中四种运输钙的蛋白质的细胞定位。然而,粗糙脉孢菌活菌丝中细胞器的结构和分布尚未得到全面描述。因此,我们构建了重组基因,这些基因产生了推定的细胞器标记蛋白与绿色或红色荧光蛋白的翻译融合体。我们在核膜和相关膜中观察到由grp - 78和dpm编码的推定内质网蛋白。由vam - 3和vma - 1编码的液泡膜蛋白存在于菌丝尖端附近由小管和小泡组成的相互连接的网络中,而在更远端的区域它们存在于大小不一的球形液泡中。用标记的ARG - 4可视化的线粒体在菌丝的所有区域都很丰富。同样,我们用绿色或红色荧光蛋白标记粗糙脉孢菌中四种运输钙的蛋白质,以研究它们的细胞定位。NCA - 1蛋白是动物细胞中SERCA型Ca(2 +)-ATP酶的同源物,与内质网标记物共定位。NCA - 2和NCA - 3蛋白分别是酵母液泡膜或动物细胞质膜中Ca(2 +)-ATP酶的同源物。它们与液泡膜标记物共定位,并且也出现在距离菌丝尖端超过1毫米区域的质膜中。cax基因编码一种存在于液泡中的Ca(2 +)/H(+)交换蛋白。正如预期的那样,CAX蛋白定位于液泡区室。我们在距离菌丝尖端约50至100微米处观察到一些球形细胞器,这些细胞器含有大量标记的CAX蛋白和液泡ATP酶的标记亚基(VMA - 1和VMA - 5)。我们认为这种以前在粗糙脉孢菌中未被描述的细胞器可能在钙的隔离中起作用。