m+Medelevator.RU
← Поиск публикаций
Proceedings of the National Academy of Sciences of the United States of America · 2026

Cellular remodeling during reversible life-stage transition in sessile ciliates: Genomic and transcriptomic insights.

СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Li Chao, Zhou Zhaorui, Wu Tong, Wang Zheng, Ji Zhongyu, Lu Borong, Zhang Xue, Lynch Michael, Yan Ying

Аннотация

Unraveling mechanisms driving dramatic life-stage transitions in response to environmental stress is central to understanding cellular adaptation. We studied a distinctive group of sessile ciliates that undergo profound morphological and organellar remodeling when transitioning from sessile trophonts to motile telotrochs. We generated chromosome-level genomes for two colonial species (Campanella sinica, Epistylis hentscheli) and one solitary species (Vorticella campanula), revealing genome sizes of 41.30 to 60.37 Mb. Notably, minichromosomes (10 to 100 kb) represent a shared, distinct chromosomal architecture across all three species. We constructed a transcriptional atlas by profiling five transitional stages, revealing core gene sets linked to transcriptional regulation, cilia, cytoskeletal dynamics, and metabolism. Intermediate stages converge on conserved genes driving structural and energetic turnover, including polyubiquitin and the mitochondrial regulator CHCHD2. Furthermore, we uncovered metabolic reprogramming and active spatial mobilization of mitochondria tailored to fuel these extreme morphological shifts. During structural remodeling, the mitochondrial genome exhibits asymmetric regulation-coordinating the upregulation of translational and early respiratory machineries with the downregulation of terminal electron transport potentially mitigating oxidative stress. Crucially, in vivo imaging physically corroborates this transcriptomic priming, revealing a marked increase in mitochondrial density and their targeted redistribution to regions of high ATP demand. Conversely, during stalk biosynthesis, organellar regulation selectively upregulates the mitochondrial protein ymf66 to sustain prolonged translational and energetic demands. Ultimately, our findings highlight how ciliates integrate global transcriptomic shifts with organelle-specific spatial and metabolic fine-tuning to meet the precise mechanical requirements of complex life-cycle transitions.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты