The HEAT repeat protein HPO-27 is a lysosome fission factor.
Letao LiXilu LiuShanshan YangMeijiao LiYanwei WuSiqi HuWenjuan WangAmin JiangQianqian ZhangJunbing ZhangXiaoli MaJunyan HuQiaohong ZhaoYubing LiuDong LiJunjie HuChonglin YangWei FengXiaochen WangPublished in: Nature (2024)
Lysosomes are degradation and signalling centres crucial for homeostasis, development and ageing 1 . To meet diverse cellular demands, lysosomes remodel their morphology and function through constant fusion and fission 2,3 . Little is known about the molecular basis of fission. Here we identify HPO-27, a conserved HEAT repeat protein, as a lysosome scission factor in Caenorhabditis elegans. Loss of HPO-27 impairs lysosome fission and leads to an excessive tubular network that ultimately collapses. HPO-27 and its human homologue MROH1 are recruited to lysosomes by RAB-7 and enriched at scission sites. Super-resolution imaging, negative-staining electron microscopy and in vitro reconstitution assays reveal that HPO-27 and MROH1 self-assemble to mediate the constriction and scission of lysosomal tubules in worms and mammalian cells, respectively, and assemble to sever supported membrane tubes in vitro. Loss of HPO-27 affects lysosomal morphology, integrity and degradation activity, which impairs animal development and longevity. Thus, HPO-27 and MROH1 act as self-assembling scission factors to maintain lysosomal homeostasis and function.
Keyphrases
- fluorescent probe
- electron microscopy
- living cells
- endothelial cells
- high resolution
- heat stress
- amino acid
- transcription factor
- neuropathic pain
- mass spectrometry
- protein protein
- physical activity
- small molecule
- single cell
- body mass index
- photodynamic therapy
- spinal cord
- high glucose
- pluripotent stem cells
- weight loss