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Different Subcellular Localization of Theiler's Murine Encephalomyelitis Virus Leader Proteins of GDVII and DA Strains in BHK-21 Cells▿

机译:GDVII和DA株的泰勒鼠脑脊髓炎病毒前导蛋白在BHK-21细胞中的不同亚细胞定位

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摘要

The highly virulent GDVII strain of Theiler's murine encephalomyelitis virus causes acute and fatal encephalomyelitis, whereas the DA strain causes mild encephalomyelitis followed by a chronic inflammatory demyelinating disease with virus persistence. The differences in the amino acid sequences of the leader protein (L) of the DA and GDVII strains are greater than those for any other viral protein. We examined the subcellular distribution of DA L and GDVII L tagged with the FLAG epitope in BHK-21 cells. Wild-type GDVII L was localized predominantly in the cytoplasm, whereas wild-type DA L showed a nucleocytoplasmic distribution. A series of the L mutant experiments demonstrated that the zinc finger domain, acidic domain, and C-terminal region of L were necessary for the nuclear accumulation of DA L. A GDVII L mutant with a deletion of the serine/threonine (S/T)-rich domain showed a nucleocytoplasmic distribution, in contrast to the predominant cytoplasmic distribution of wild-type GDVII L. A chimeric DA/GDVII L, D/G, which encodes the N region of DA L including the zinc finger domain and acidic domain, followed by the GDVII L sequence including the S/T-rich domain, was distributed exclusively throughout the cytoplasm but not in the nucleus, as observed with wild-type GDVII L. Another chimeric L, G/D (which is the converse of the D/G construct), accumulated in the nucleus as well as the cytoplasm, as was observed for wild-type DA L. The findings suggest that the differential distribution of DA L and GDVII L is determined primarily by the S/T-rich domain. The S/T-rich domain may be important for the viral activity through the regulation of the subcellular distribution of L.
机译:泰勒氏鼠脑脊髓炎病毒的高毒力GDVII株会引起急性和致命性脑脊髓炎,而DA株会导致轻度脑脊髓炎,然后是病毒持续存在的慢性炎症性脱髓鞘疾病。 DA和GDVII株的前导蛋白(L)氨基酸序列的差异大于任何其他病毒蛋白。我们检查了用BAG-21细胞中的FLAG表位标记的DA L和GDVII L的亚细胞分布。野生型GDVII L主要位于细胞质中,而野生型DA L显示出核质分布。一系列L突变实验表明,L的锌指结构域,酸性结构域和C末端区域对于DA L的核积累是必需的。一个带有丝氨酸/苏氨酸缺失的GDVII L突变体(S / T与野生型GDVII L的主要胞质分布相反,富含)的域显示了胞质分布。嵌合的DA / GDVII L,D / G编码DA L的N区,包括锌指结构域和酸性结构域如野生型GDVII L所观察到的,随后是包含S / T富集结构域的GDVII L序列仅分布在整个细胞质中,而不是分布在细胞核中。另一种嵌合L,G / D(与D / G构建体),如野生型DA L所观察到的那样,积累在细胞核和细胞质中。研究结果表明,DA L和GDVII L的差异分布主要取决于富含S / T的域。通过调节L的亚细胞分布,富含S / T的结构域对于病毒活性可能是重要的。

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