Boswell Leaf C, Hand Steven C
Division of Cellular, Developmental and Integrative Biology, Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, United States.
Division of Cellular, Developmental and Integrative Biology, Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, United States.
Tissue Cell. 2014 Dec;46(6):514-9. doi: 10.1016/j.tice.2014.09.004. Epub 2014 Sep 19.
Late embryogenesis abundant (LEA) proteins are accumulated by anhydrobiotic organisms in response to desiccation and improve survivorship during water stress. In this study we provide the first direct evidence for the subcellular localizations of AfrLEA2 and AfrLEA3m (and its subforms) in anhydrobiotic embryos of Artemia franciscana. Immunohistochemistry shows AfrLEA2 to reside in the cytoplasm and nucleus, and the four AfrLEA3m proteins to be localized to the mitochondrion. Cellular locations are supported by Western blots of mitochondrial, nuclear and cytoplasmic fractions. The presence of LEA proteins in multiple subcellular compartments of A. franciscana embryos suggests the need to protect biological structures in many areas of a cell in order for an organism to survive desiccation stress, and may explain in part why a multitude of different LEA proteins are expressed by a single organism.
晚期胚胎发生丰富(LEA)蛋白由脱水生物在响应干燥时积累,并在水分胁迫期间提高存活率。在本研究中,我们首次提供了AfrLEA2和AfrLEA3m(及其亚型)在卤虫脱水胚胎中亚细胞定位的直接证据。免疫组织化学显示AfrLEA2存在于细胞质和细胞核中,而四种AfrLEA3m蛋白定位于线粒体。线粒体、细胞核和细胞质组分的蛋白质印迹法证实了这些细胞定位。卤虫胚胎多个亚细胞区室中存在LEA蛋白,表明为使生物体在干燥胁迫下存活,需要保护细胞许多区域的生物结构,这可能部分解释了为什么单个生物体表达多种不同的LEA蛋白。