TUMOVA, P., L. VOLEMAN, A. KLINGL, E. NOHYNKOVA, G. WANNER and P. DOLEZAL. Inheritance of the reduced mitochondria of Giardia intestinalis is coupled to the flagellar maturation cycle. BMC BIOLOGY. 2021, vol. 19, No 1, p. 193-212. ISSN 1741-7007. Available from: https://dx.doi.org/10.1186/s12915-021-01129-7.
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Basic information
Original name Inheritance of the reduced mitochondria of Giardia intestinalis is coupled to the flagellar maturation cycle
Authors TUMOVA, P., L. VOLEMAN, A. KLINGL, E. NOHYNKOVA, G. WANNER and P. DOLEZAL.
Edition BMC BIOLOGY, 2021, 1741-7007.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10600 1.6 Biological sciences
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 7.364
RIV identification code RIV/00216224:14740/21:00124513
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1186/s12915-021-01129-7
UT WoS 000695452800005
Keywords in English Mitochondrial inheritanceMitosomesmitochondrial evolutionFlagellumCytoskeletonCell cycleMitochondrial divisionProtistGiardia
Tags ne MU, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 18/5/2022 15:04.
Abstract
Background The presence of mitochondria is a distinguishing feature between prokaryotic and eukaryotic cells. It is currently accepted that the evolutionary origin of mitochondria coincided with the formation of eukaryotes and from that point control of mitochondrial inheritance was required. Yet, the way the mitochondrial presence has been maintained throughout the eukaryotic cell cycle remains a matter of study. Eukaryotes control mitochondrial inheritance mainly due to the presence of the genetic component; still only little is known about the segregation of mitochondria to daughter cells during cell division. Additionally, anaerobic eukaryotic microbes evolved a variety of genomeless mitochondria-related organelles (MROs), which could be theoretically assembled de novo, providing a distinct mechanistic basis for maintenance of stable mitochondrial numbers. Here, we approach this problem by studying the structure and inheritance of the protist Giardia intestinalis MROs known as mitosomes. Results We combined 2D stimulated emission depletion (STED) microscopy and focused ion beam scanning electron microscopy (FIB/SEM) to show that mitosomes exhibit internal segmentation and conserved asymmetric structure. From a total of about forty mitosomes, a small, privileged population is harnessed to the flagellar apparatus, and their life cycle is coordinated with the maturation cycle of G. intestinalis flagella. The orchestration of mitosomal inheritance with the flagellar maturation cycle is mediated by a microtubular connecting fiber, which physically links the privileged mitosomes to both axonemes of the oldest flagella pair and guarantees faithful segregation of the mitosomes into the daughter cells. Conclusion Inheritance of privileged Giardia mitosomes is coupled to the flagellar maturation cycle. We propose that the flagellar system controls segregation of mitochondrial organelles also in other members of this supergroup (Metamonada) of eukaryotes and perhaps reflects the original strategy of early eukaryotic cells to maintain this key organelle before mitochondrial fusion-fission dynamics cycle as observed in Metazoa was established.
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