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Updated: Jan 23, 2026

The Plant Infection Test: Spray and Wound-Mediated Inoculation with the Plant Pathogen Magnaporthe Grisea
Published on: August 4, 2018
ATG5-HSP90.2-mediated micromitophagy as a cytological basis for maternal inheritance of plant mitochondria
Xiaorong Huang1,2, Linlin Zhao3,4, Zonglin Liu3
1State Key Laboratory of Hybrid Rice, College of Life Sciences, Wuhan University, Wuhan, China. huangxr@xmu.edu.cn.
Abstract:
Mitochondria are inherited maternally in most plants as a classical paradigm of non-Mendelian inheritance, but the mechanism underlying paternal mitochondrial elimination (PME) remains almost unknown. We report here that angiosperms have evolved micromitophagy-mediated PME, in which vacuoles directly engulf paternal mitochondria via tonoplast invagination. We show that micromitophagy occurs specifically in male germline (MG) cells. To gain mechanistic insights, we used a vegetative-to-germline cell fate transition system to establish that micromitophagy is triggered by MG cell fate determination. We found evidence that ATG5 is translocated to vacuoles upon MG-cell-fate determination and interacts with mitochondrion-located HSP90.2 during mitochondrial engulfment by vacuoles, elucidating a cell-type-specific ATG neofunctionalization to mediate micromitophagy. This mechanism not only contributes to maternal inheritance of plant mitochondria but also supports the zygote-to-embryo transition. We further determined that micromitophagy is conserved in angiosperms but was continually optimized during evolution to support the best functioning of PME in MG cells with different properties. These findings bridge a long-standing gap in understanding plant PME with emerging mechanistic knowledge.
Insights
Plants eliminate paternal mitochondria using micromitophagy, a process where vacuoles engulf them in male germline cells. This mechanism, involving ATG5 and HSP90.2, ensures maternal mitochondrial inheritance and is conserved across angiosperms.
Area of Science:
- Plant biology
- Cell biology
- Genetics
Background:
- Mitochondria are typically maternally inherited in plants, a key aspect of non-Mendelian inheritance.
- The precise mechanisms driving paternal mitochondrial elimination (PME) in plants are not well understood.
Purpose of the Study:
- To elucidate the molecular and cellular mechanisms of paternal mitochondrial elimination (PME) in angiosperms.
- To investigate the role of autophagy-related proteins in PME.
Main Methods:
- Utilized a vegetative-to-germline cell fate transition system in plants.
- Investigated the translocation and interaction of ATG5 and HSP90.2.
- Observed vacuolar engulfment of paternal mitochondria via tonoplast invagination.
Main Results:
- Discovered that angiosperms employ micromitophagy-mediated PME, involving direct engulfment of paternal mitochondria by vacuoles in male germline (MG) cells.
- Demonstrated that micromitophagy is triggered by male germline cell fate determination.
- Showed that ATG5 translocates to vacuoles and interacts with mitochondrion-located HSP90.2 during this process, revealing cell-type-specific ATG neofunctionalization.
Conclusions:
- Micromitophagy is the primary mechanism for PME in angiosperms, ensuring maternal mitochondrial inheritance.
- This process is conserved and optimized throughout angiosperm evolution.
- The findings provide crucial mechanistic insights into plant PME and support zygote-to-embryo transition.
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