Electron microscopic observation revealed that poplar (Populus deltoides Marsh.) and winterwheat ( Triticum aestivum L. cv. Seward 80004) plasmodesmatal structures significantly changed undershort day (SD, 8 h light) ...Electron microscopic observation revealed that poplar (Populus deltoides Marsh.) and winterwheat ( Triticum aestivum L. cv. Seward 80004) plasmodesmatal structures significantly changed undershort day (SD, 8 h light) and in winter period, and such changes differed also noticeably between these twowoody and herbaceous plants. Under long day (LD, 16 h light), many plasmodesmata with strong stainappeared in the cell wall of both poplar apical buds and winter wheat young leaf tissues, and connections ofcytoplasmic endoplasmic reticulum (ER) with the ER in some plasmodesmata were observed. In addition,the typical “neck type” plasmodesmata were observed in winter wheat young leaf tissues, and their centraldesmotubules (appressed-ER) could be clearly identified. Under SD, many poplar plasmodesmata showedonly a partial structure in the cell wall and appeared to be discontinued; some plasmodesmata swelled in themid-wall, forming the cavity, and no appressed-ER appeared, in winter wheat, however, no noticeablealterations of plasmodesmata occurred, and the plasmodesmatal structure essentially remained the sameas it was under LD. In winter period, poplar plasmodesmata had a similar morphology as those observedunder SD, however, winter wheat manifested at least two types of significant plasmodesmatal alterations:one plugged by electron-dense materials and the other of reduced neck region compared to those underLD. The above dynamic difference of the two species plasmodesmata under SD and winter period revealedthe difference of their dormancy development under those environmental conditions.展开更多
The herpes simplex virus type 1 （HSV-1） VP22, is one of the most abundant HSV-I tegument proteins with an average stoichiometry of 2 400 copies per virion and conserved among alphaherpesvirinae. Many functions are a...The herpes simplex virus type 1 （HSV-1） VP22, is one of the most abundant HSV-I tegument proteins with an average stoichiometry of 2 400 copies per virion and conserved among alphaherpesvirinae. Many functions are attributed to VP22, including nuclear localization, chromatin binding, microtubule binding, induction ofmicrotubule reorganization, intercellular transport, interaction with cellular proteins, such as template activating VP16, pU factor I （TAF-I） and nonmuscle myosin II A （NMIIA）, and viral proteins including pUS9 and pUL46, glycoprotein E （gE） and gD. Recently, many novel functions perform tegument protein ed by the HSV-1 VP22 protein have been shown, including promotion of protein synthesis at late times in infection, accumulation of a subset of viral mRNAs at early times in infection and possible transcriptional regulation function .展开更多
Plasmodesmata (PDs) are cytoplasmic structures that link adjacent cells to form the symplast of a plant. PDs are involved extensively in a plant's life by mediating symplastic transport of a wide range of ions and...Plasmodesmata (PDs) are cytoplasmic structures that link adjacent cells to form the symplast of a plant. PDs are involved extensively in a plant's life by mediating symplastic transport of a wide range of ions and molecules. Major components of a plasmodesma (PD) include a plasma membrane, a desmotubule, and a cytoplasmic annulus, all of which are readily detectable by electron microscopy. Both the plasma membrane and the desmotubule contain proteinaceous particles, thought to be involved in altering the size of the cytoplasmic annulus. Cytoskeleton elements (actin and myosin) are essential for maintaining the integrity of PDs. Together with these elements, calcium_binding proteins probably play a significant role in regulating PD function. Symplastic transport occurs through the cytoplasmic annulus for the great majority of solutes, while other substances may traverse through the desmotubule internal compartment, the desmotubule shell, or the plasma membrane. The symplast is subdivided into several domains with varying molecular size exclusion limits (ranging from <1 kD to >10 kD). Plasmodesmata can be either primary or secondary; the former are developed during new wall formation and the latter are made in existing walls. The dynamic nature of plasmodesmata is also reflected by their changing frequencies, which, in turn, depend on the developmental and physiological status of the tissue or the entire plant. While diffusion is the major mechanism of symplastic transport, plasmodesmata are selective for certain ions and molecules. Upon viral infection, viral movement proteins interact with PD receptor proteins and, as a result of yet unknown mechanisms, the plasmodesmata are remarkably dilated to allow viral movement proteins and the bound viral genome to enter healthy cells. Some proteins of plant origin are also able to traverse plasmodesmata, presumably in ways similar to viral movement proteins. Some of these plant proteins are probably signal molecules contributing to cell differentiation and other activities. Other proteins move cell_to_cell in a non_specific manner.展开更多
文摘Electron microscopic observation revealed that poplar (Populus deltoides Marsh.) and winterwheat ( Triticum aestivum L. cv. Seward 80004) plasmodesmatal structures significantly changed undershort day (SD, 8 h light) and in winter period, and such changes differed also noticeably between these twowoody and herbaceous plants. Under long day (LD, 16 h light), many plasmodesmata with strong stainappeared in the cell wall of both poplar apical buds and winter wheat young leaf tissues, and connections ofcytoplasmic endoplasmic reticulum (ER) with the ER in some plasmodesmata were observed. In addition,the typical “neck type” plasmodesmata were observed in winter wheat young leaf tissues, and their centraldesmotubules (appressed-ER) could be clearly identified. Under SD, many poplar plasmodesmata showedonly a partial structure in the cell wall and appeared to be discontinued; some plasmodesmata swelled in themid-wall, forming the cavity, and no appressed-ER appeared, in winter wheat, however, no noticeablealterations of plasmodesmata occurred, and the plasmodesmatal structure essentially remained the sameas it was under LD. In winter period, poplar plasmodesmata had a similar morphology as those observedunder SD, however, winter wheat manifested at least two types of significant plasmodesmatal alterations:one plugged by electron-dense materials and the other of reduced neck region compared to those underLD. The above dynamic difference of the two species plasmodesmata under SD and winter period revealedthe difference of their dormancy development under those environmental conditions.
基金The Startup Fund of the Hundred Talents Program of the Chinese Academy of Science (20071010- 141)National Natural Science Foundation of China (30870120)Open Research Fund Program of the State Key Laboratory of Virology of China (2007003, 2009007)
文摘The herpes simplex virus type 1 （HSV-1） VP22, is one of the most abundant HSV-I tegument proteins with an average stoichiometry of 2 400 copies per virion and conserved among alphaherpesvirinae. Many functions are attributed to VP22, including nuclear localization, chromatin binding, microtubule binding, induction ofmicrotubule reorganization, intercellular transport, interaction with cellular proteins, such as template activating VP16, pU factor I （TAF-I） and nonmuscle myosin II A （NMIIA）, and viral proteins including pUS9 and pUL46, glycoprotein E （gE） and gD. Recently, many novel functions perform tegument protein ed by the HSV-1 VP22 protein have been shown, including promotion of protein synthesis at late times in infection, accumulation of a subset of viral mRNAs at early times in infection and possible transcriptional regulation function .
文摘Plasmodesmata (PDs) are cytoplasmic structures that link adjacent cells to form the symplast of a plant. PDs are involved extensively in a plant's life by mediating symplastic transport of a wide range of ions and molecules. Major components of a plasmodesma (PD) include a plasma membrane, a desmotubule, and a cytoplasmic annulus, all of which are readily detectable by electron microscopy. Both the plasma membrane and the desmotubule contain proteinaceous particles, thought to be involved in altering the size of the cytoplasmic annulus. Cytoskeleton elements (actin and myosin) are essential for maintaining the integrity of PDs. Together with these elements, calcium_binding proteins probably play a significant role in regulating PD function. Symplastic transport occurs through the cytoplasmic annulus for the great majority of solutes, while other substances may traverse through the desmotubule internal compartment, the desmotubule shell, or the plasma membrane. The symplast is subdivided into several domains with varying molecular size exclusion limits (ranging from <1 kD to >10 kD). Plasmodesmata can be either primary or secondary; the former are developed during new wall formation and the latter are made in existing walls. The dynamic nature of plasmodesmata is also reflected by their changing frequencies, which, in turn, depend on the developmental and physiological status of the tissue or the entire plant. While diffusion is the major mechanism of symplastic transport, plasmodesmata are selective for certain ions and molecules. Upon viral infection, viral movement proteins interact with PD receptor proteins and, as a result of yet unknown mechanisms, the plasmodesmata are remarkably dilated to allow viral movement proteins and the bound viral genome to enter healthy cells. Some proteins of plant origin are also able to traverse plasmodesmata, presumably in ways similar to viral movement proteins. Some of these plant proteins are probably signal molecules contributing to cell differentiation and other activities. Other proteins move cell_to_cell in a non_specific manner.
