Intra-Golgi Golgin <i>Pp</i>Sgm1 and GRIP domain Golgin <i>Pp</i>Imh1 synergistically mediate Golgi cisternal stacking

Regulation of the distinctive stacked Golgi morphology remains an unresolved subject. Using the budding yeast Pichia pastoris, we have previously documented the role of GRIP domain Golgin P. pastoris (Pp)Imh1 in cisternal stacking, regulated by the Arl3-Arl1 GTPase cascade switch. Expanding our work with the present study, we demonstrate the participation of PpSgm1, another conserved Golgin, in this stacking process alongside PpImh1. Null mutation of P. pastoris SGM1 caused partial unstacking of the late cisternae from the Golgi stack, implicating its role in cisternal stacking. When we overexpressed PpImh1 or PpSgm1 independently, each failed to restore stacking in the absence of the other, suggesting neither of them is sufficient for cisternal stacking alone. On the other hand, a double knockout of PpIMH1 and PpSGM1 led to a dramatic phenotype, causing complete separation of the late cisternae from the Golgi stack and significantly increasing TGN peeling, as seen in electron microscopy and live-cell imaging. Our results suggest a synergistic collaboration of PpImh1 and PpSgm1 in cisternal stacking, with implications for a conserved mechanism across species.

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Publication Details

Journal
Journal of Cell Science
Published
2025-04-24
DOI
https://doi.org/10.1242/jcs.263612
Citations
1
Primary Topic
Cellular transport and secretion
Type
article
Field-Weighted Citation Impact
1.15
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article

Intra-Golgi Golgin PpSgm1 and GRIP domain Golgin PpImh1 synergistically mediate Golgi cisternal stacking

Dibyendu Bhattacharyya, Roma Dahara
1 citations
Journal of Cell Science
Cellular transport and secretion
1.15
article

Intra-Golgi Golgin PpSgm1 and GRIP domain Golgin PpImh1 synergistically mediate Golgi cisternal stacking

Dibyendu Bhattacharyya, Roma Dahara
article en
1 citations

Abstract

Regulation of the distinctive stacked Golgi morphology remains an unresolved subject. Using the budding yeast Pichia pastoris, we have previously documented the role of GRIP domain Golgin P. pastoris (Pp)Imh1 in cisternal stacking, regulated by the Arl3-Arl1 GTPase cascade switch. Expanding our work with the present study, we demonstrate the participation of PpSgm1, another conserved Golgin, in this stacking process alongside PpImh1. Null mutation of P. pastoris SGM1 caused partial unstacking of the late cisternae from the Golgi stack, implicating its role in cisternal stacking. When we overexpressed PpImh1 or PpSgm1 independently, each failed to restore stacking in the absence of the other, suggesting neither of them is sufficient for cisternal stacking alone. On the other hand, a double knockout of PpIMH1 and PpSGM1 led to a dramatic phenotype, causing complete separation of the late cisternae from the Golgi stack and significantly increasing TGN peeling, as seen in electron microscopy and live-cell imaging. Our results suggest a synergistic collaboration of PpImh1 and PpSgm1 in cisternal stacking, with implications for a conserved mechanism across species.

Journal of Cell ScienceVol. 138(11)
Environmental Research Institute of Michigan (US), Homi Bhabha National Institute (IN), University of Michigan (US), Tata Memorial Hospital (IN), Advanced Centre for Treatment, Research and Education in Cancer (IN)
Life in Land
Openalex Percentile: Top 25%
Cellular transport and secretion
1.15
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