MTV proteins unveil ER- and microtubule-associated compartments in the plant vacuolar trafficking pathway.
basic_science · Level V
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- Record sourced from PubMed, PMID 32321832.
- Also identified by DOI 10.1073/pnas.1919820117 and PMC identifier 7211965.
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Abstract
The factors and mechanisms involved in vacuolar transport in plants, and in particular those directing vesicles to their target endomembrane compartment, remain largely unknown. To identify components of the vacuolar trafficking machinery, we searched for <i>Arabidopsis modified transport to the vacuole</i> (<i>mtv</i>) mutants that abnormally secrete the synthetic vacuolar cargo VAC2. We report here on the identification of 17 <i>mtv</i> mutations, corresponding to mutant alleles of <i>MTV2/VSR4</i>, <i>MTV3/PTEN2A MTV7/EREL1</i>, <i>MTV8/ARFC1</i>, <i>MTV9/PUF2</i>, <i>MTV10/VPS3</i>, <i>MTV11/VPS15</i>, <i>MTV12/GRV2</i>, <i>MTV14/GFS10</i>, <i>MTV15/BET11</i>, <i>MTV16/VPS51</i>, <i>MTV17/VPS54</i>, and <i>MTV18/VSR1</i> Eight of the MTV proteins localize at the interface between the <i>trans</i>-Golgi network (TGN) and the multivesicular bodies (MVBs), supporting that the trafficking step between these compartments is essential for segregating vacuolar proteins from those destined for secretion. Importantly, the GARP tethering complex subunits MTV16/VPS51 and MTV17/VPS54 were found at endoplasmic reticulum (ER)- and microtubule-associated compartments (EMACs). Moreover, MTV16/VPS51 interacts with the motor domain of kinesins, suggesting that, in addition to tethering vesicles, the GARP complex may regulate the motors that transport them. Our findings unveil a previously uncharacterized compartment of the plant vacuolar trafficking pathway and support a role for microtubules and kinesins in GARP-dependent transport of soluble vacuolar cargo in plants.
Medical subject headings
- Arabidopsis Proteins
- Protein Transport
- Vacuoles
- Vesicular Transport Proteins