A novel nabelschnur protein regulates segregation of the kinetoplast DNA in Trypanosoma brucei
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F24%3A00603905" target="_blank" >RIV/60077344:_____/24:00603905 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61988987:17310/24:A25039N3 RIV/60076658:12310/24:43909128
Výsledek na webu
<a href="https://doi.org/10.1016/j.cub.2024.08.044" target="_blank" >https://doi.org/10.1016/j.cub.2024.08.044</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.cub.2024.08.044" target="_blank" >10.1016/j.cub.2024.08.044</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
A novel nabelschnur protein regulates segregation of the kinetoplast DNA in Trypanosoma brucei
Popis výsledku v původním jazyce
The acquisition of mitochondria was imperative for initiating eukaryogenesis and thus is a characteristic feature of eukaryotic cells.1,2 The parasitic protist Trypanosoma brucei contains a singular mitochondrion with a unique mitochondrial genome, termed the kinetoplast DNA (kDNA).3 Replication of the kDNA occurs during the G1 phase of the cell cycle, prior to the start of nuclear DNA replication.4 Although numerous proteins have been functionally characterized and identified as vital components of kDNA replication and division, the molecular mechanisms governing this highly precise process remain largely unknown.5,6 One division-related and morphologically characteristic structure that remains most enigmatic is the nabelschnur, an undefined, filament-resembling structure observed by electron microscopy between segregating daughter kDNA networks.7-9 To date, only one protein, TbLAP1, an M17 family leucyl aminopeptidase metalloprotease, is known to localize to the nabelschnur.9 While screening proteins from the T. brucei MitoTag project,10 we identified a previously uncharacterized protein with an mNeonGreen signal localizing to the kDNA as well as forming a point of connection between dividing kDNAs. Here, we demonstrate that this kDNA-associated protein, named TbNAB70, indeed localizes to the nabelschnur and plays an essential role in the segregation of newly replicated kDNAs and subsequent cytokinesis in T. brucei.
Název v anglickém jazyce
A novel nabelschnur protein regulates segregation of the kinetoplast DNA in Trypanosoma brucei
Popis výsledku anglicky
The acquisition of mitochondria was imperative for initiating eukaryogenesis and thus is a characteristic feature of eukaryotic cells.1,2 The parasitic protist Trypanosoma brucei contains a singular mitochondrion with a unique mitochondrial genome, termed the kinetoplast DNA (kDNA).3 Replication of the kDNA occurs during the G1 phase of the cell cycle, prior to the start of nuclear DNA replication.4 Although numerous proteins have been functionally characterized and identified as vital components of kDNA replication and division, the molecular mechanisms governing this highly precise process remain largely unknown.5,6 One division-related and morphologically characteristic structure that remains most enigmatic is the nabelschnur, an undefined, filament-resembling structure observed by electron microscopy between segregating daughter kDNA networks.7-9 To date, only one protein, TbLAP1, an M17 family leucyl aminopeptidase metalloprotease, is known to localize to the nabelschnur.9 While screening proteins from the T. brucei MitoTag project,10 we identified a previously uncharacterized protein with an mNeonGreen signal localizing to the kDNA as well as forming a point of connection between dividing kDNAs. Here, we demonstrate that this kDNA-associated protein, named TbNAB70, indeed localizes to the nabelschnur and plays an essential role in the segregation of newly replicated kDNAs and subsequent cytokinesis in T. brucei.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10608 - Biochemistry and molecular biology
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2024
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Current Biology
ISSN
0960-9822
e-ISSN
1879-0445
Svazek periodika
34
Číslo periodika v rámci svazku
20
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
14
Strana od-do
4803-4812
Kód UT WoS článku
001388001900001
EID výsledku v databázi Scopus
2-s2.0-85207472404