The function of GORASPs in Golgi apparatus organization in vivo

Rianne Grond; Tineke Veenendaal; Juan M Duran; Ishier Raote; Johan H van Es; Sebastiaan Corstjens; Laura Delfgou; Benaissa El Haddouti; Vivek Malhotra; Catherine Rabouille

doi:10.1083/jcb.202004191

The function of GORASPs in Golgi apparatus organization in vivo

Rianne Grond, Tineke Veenendaal, Juan M Duran, Ishier Raote, Johan H van Es, Sebastiaan Corstjens, Laura Delfgou, Benaissa El Haddouti, Vivek Malhotra, Catherine Rabouille

Hubrecht Institute

Onderzoeksoutput: Bijdrage aan wetenschappelijk tijdschrift/periodieke uitgave › Artikel › Wetenschappelijk › peer review

26 Citaten (Scopus)

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In vitro experiments have shown that GRASP65 (GORASP1) and GRASP55 (GORASP2) proteins function in stacking Golgi cisternae. However, in vivo depletion of GORASPs in metazoans has given equivocal results. We have generated a mouse lacking both GORASPs and find that Golgi cisternae remained stacked. However, the stacks are disconnected laterally from each other, and the cisternal cross-sectional diameters are significantly reduced compared with their normal counterparts. These data support earlier findings on the role of GORASPs in linking stacks, and we suggest that unlinking of stacks likely affects dynamic control of COPI budding and vesicle fusion at the rims. The net result is that cisternal cores remain stacked, but cisternal diameter is reduced by rim consumption.

Originele taal-2	Engels
Tijdschrift	Journal of Cell Biology
Volume	219
Nummer van het tijdschrift	9
DOI's	https://doi.org/10.1083/jcb.202004191
Status	Gepubliceerd - 07 sep. 2020

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title = "The function of GORASPs in Golgi apparatus organization in vivo",

abstract = "In vitro experiments have shown that GRASP65 (GORASP1) and GRASP55 (GORASP2) proteins function in stacking Golgi cisternae. However, in vivo depletion of GORASPs in metazoans has given equivocal results. We have generated a mouse lacking both GORASPs and find that Golgi cisternae remained stacked. However, the stacks are disconnected laterally from each other, and the cisternal cross-sectional diameters are significantly reduced compared with their normal counterparts. These data support earlier findings on the role of GORASPs in linking stacks, and we suggest that unlinking of stacks likely affects dynamic control of COPI budding and vesicle fusion at the rims. The net result is that cisternal cores remain stacked, but cisternal diameter is reduced by rim consumption.",

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AU - Grond, Rianne

AU - Veenendaal, Tineke

AU - Duran, Juan M

AU - Raote, Ishier

AU - van Es, Johan H

AU - Corstjens, Sebastiaan

AU - Delfgou, Laura

AU - El Haddouti, Benaissa

AU - Malhotra, Vivek

AU - Rabouille, Catherine

PY - 2020/9/7

Y1 - 2020/9/7

N2 - In vitro experiments have shown that GRASP65 (GORASP1) and GRASP55 (GORASP2) proteins function in stacking Golgi cisternae. However, in vivo depletion of GORASPs in metazoans has given equivocal results. We have generated a mouse lacking both GORASPs and find that Golgi cisternae remained stacked. However, the stacks are disconnected laterally from each other, and the cisternal cross-sectional diameters are significantly reduced compared with their normal counterparts. These data support earlier findings on the role of GORASPs in linking stacks, and we suggest that unlinking of stacks likely affects dynamic control of COPI budding and vesicle fusion at the rims. The net result is that cisternal cores remain stacked, but cisternal diameter is reduced by rim consumption.

AB - In vitro experiments have shown that GRASP65 (GORASP1) and GRASP55 (GORASP2) proteins function in stacking Golgi cisternae. However, in vivo depletion of GORASPs in metazoans has given equivocal results. We have generated a mouse lacking both GORASPs and find that Golgi cisternae remained stacked. However, the stacks are disconnected laterally from each other, and the cisternal cross-sectional diameters are significantly reduced compared with their normal counterparts. These data support earlier findings on the role of GORASPs in linking stacks, and we suggest that unlinking of stacks likely affects dynamic control of COPI budding and vesicle fusion at the rims. The net result is that cisternal cores remain stacked, but cisternal diameter is reduced by rim consumption.

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DO - 10.1083/jcb.202004191

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JO - Journal of Cell Biology

JF - Journal of Cell Biology

IS - 9

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The function of GORASPs in Golgi apparatus organization in vivo

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