PT - JOURNAL ARTICLE AU - Arya Bagus Boedi Iswanto AU - Minh Huy Vu AU - Ritesh Kumar AU - Jong Cheol Shon AU - Shuwei Wu AU - Da-Ran Kim AU - Kwak Yeon Sik AU - Son Geon Hui AU - Hobin Kang AU - Woe Yoen Kim AU - Sang Hee Kim AU - Kwang Hyeon Liu AU - Jae-Yean Kim TI - α1-COP delivers sphingolipid modifiers and controls plasmodesmal callose deposition in Arabidopsis AID - 10.1101/2021.03.22.436362 DP - 2021 Jan 01 TA - bioRxiv PG - 2021.03.22.436362 4099 - http://biorxiv.org/content/early/2021/03/22/2021.03.22.436362.short 4100 - http://biorxiv.org/content/early/2021/03/22/2021.03.22.436362.full AB - Callose is a plant cell wall polymer in the form of β-1,3-glucan, which regulates symplasmic channel size at plasmodesmata (PD). It plays a crucial role in a variety of processes in plants through the regulation of intercelluar symplasmic continuity. However, how to maintain callose homeostasis at PD in the molecular levels is poorly understood. To further elucidate the mechanism of PD callose homeostasis, we screened and identified an Arabidopsis mutant plant that exhibited excessive callose deposition at PD. Based on the Next-generation sequencing (NGS)-based mapping, other mutant allele analysis, and complementation assay, the mutated gene was shown to be α1-COP, which encodes a member of the COPI coatomer complex comprised of α, β, β′, γ, δ, ε, and ζ subunits. Since there is no report on the link between COPI and callose/PD, it was extremely curious to know the roles of α1-COP or COPI in PD regulation through callose deposition. Here, we report that loss-of-function of α1-COP directly elevates the callose accumulation at PD by affecting subcellular protein localization of callose degradation enzyme PdBG2. This process is linked to ERH1, an inositol phosphoryl ceramide synthase (IPCS), and glucosylceramide synthase (GCS) functions through physical interactions with the α1-COP protein. In addition, the loss-of-function of α1-COP also alters the subcellular localization of ERH1 and GCS proteins, results in a reduction of GlcCers and GlcHCers molecules, which are the key SL species for lipid raft formation. According to our findings, we propose that α1-COP protein, together with the SL modifiers controlling lipid raft compositions, regulates the function of GPI-anchored PD proteins and hence the callose turnover at PD and symplastic movement of biomolecules. Our findings provide the first key clue to link the COPI-mediated intracellular trafficking pathway to the callose-mediated intercellular signaling pathway through PD.One-sentence summary Plant-specific coatomer protein functions as a negative regulator of callose accumulation by regulating the translocation of sphingolipid enzymes.Competing Interest StatementThe authors have declared no competing interest.