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  • 1
    Online Resource
    Online Resource
    Walter de Gruyter GmbH ; 2015
    In:  Biological Chemistry Vol. 396, No. 5 ( 2015-05-1), p. 495-509
    In: Biological Chemistry, Walter de Gruyter GmbH, Vol. 396, No. 5 ( 2015-05-1), p. 495-509
    Abstract: Glutaredoxins (GRXs) are small oxidoreductases of the thioredoxin family proteins that can either regulate the thiol redox state of proteins or are linked to iron metabolism because of their ability to incorporate iron-sulfur [2Fe–2S] clusters. Here we review recent research on a land plant-specific class of GRX-like proteins, which are characterized by the conserved CC motif in the active centre. Loss-of-function mutants of CC-type GRXs in Arabidopsis (also named ROXYs), maize, and rice have unraveled a role in floral development, including regulation of organ primordia initiation, control of organ identity gene expression, and progression into meiosis in the male germ line. Other CC-type GRXs play a role in stress responses, most likely through their capacity to regulate nuclear gene expression. Consistently, CC-type GRXs, physically and genetically interact with individual members of the TGA transcription factor family. One of the challenges in the future is to unravel whether ROXYs control the redox state of TGA factors or other yet unknown target proteins or whether they regulate gene expression through other processes. Other intriguing questions concern the original function of the first CC-type GRXs in basal land plants and their potential contribution to the extremely successful radiation of angiosperms.
    Type of Medium: Online Resource
    ISSN: 1437-4315 , 1431-6730
    Language: Unknown
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2015
    detail.hit.zdb_id: 1466062-3
    SSG: 12
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  • 2
    In: American Journal of Physiology-Cell Physiology, American Physiological Society, Vol. 291, No. 4 ( 2006-10), p. C710-C717
    Abstract: Eryptosis or apoptosis-like death of erythrocytes is characterized by phosphatidylserine exposure and erythrocyte shrinkage, both typical features of nucleated apoptotic cells. Eryptosis is triggered by activation of nonselective Ca 2+ -permeable cation channels with subsequent entry of Ca 2+ and stimulation of Ca 2+ -sensitive scrambling of the cell membrane. The channels are activated and thus eryptosis is triggered by Cl − removal, osmotic shock, oxidative stress, or glucose deprivation. The present study has been performed to compare cation channel activity and susceptibility to eryptosis in neonatal and adult erythrocytes. Channel activity was determined by patch-clamp analysis, cytosolic Ca 2+ activity by fluo-3 fluorescence, phosphatidylserine exposure by FITC-labeled annexin V binding, and cell shrinkage by decrease in forward scatter in fluorescence-activated cell sorting analysis. Prostaglandin E 2 (PGE 2 ) formation, cation channel activity, Ca 2+ entry, annexin V binding, and decreased forward scatter were triggered by removal of Cl − in both adult and neonatal erythrocytes. The effects were, however, significantly blunted in neonatal erythrocytes. Osmotic shock, PGE 2, and platelet-activating factor similarly increased annexin V binding and decreased forward scatter, effects again significantly reduced in neonatal erythrocytes. On the other hand, spontaneous and oxidative (addition of tert-butylperoxide) stress-induced eryptosis was significantly larger in neonatal erythrocytes. In conclusion, cation channel activity, Ca 2+ leakage, and thus channel-dependent triggering of eryptosis are blunted, whereas spontaneous and oxidative stress-induced eryptosis is more pronounced in neonatal erythrocytes.
    Type of Medium: Online Resource
    ISSN: 0363-6143 , 1522-1563
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2006
    detail.hit.zdb_id: 1477334-X
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    S. Karger AG ; 2007
    In:  Cellular Physiology and Biochemistry Vol. 19, No. 1-4 ( 2007), p. 175-184
    In: Cellular Physiology and Biochemistry, S. Karger AG, Vol. 19, No. 1-4 ( 2007), p. 175-184
    Type of Medium: Online Resource
    ISSN: 1015-8987 , 1421-9778
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2007
    detail.hit.zdb_id: 1482056-0
    SSG: 12
    SSG: 15,3
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