Two paralogous PHD finger proteins participate in natural genome editing in <i>Paramecium tetraurelia</i>

The unicellular eukaryote Paramecium tetraurelia contains functionally distinct nuclei: germline micronuclei (MICs) and a somatic macronucleus (MAC). During sex, the MIC genome is reorganized into a new MAC genome and the old MAC is lost. Almost 45,000 unique internal eliminated sequences (IESs) distributed throughout the genome require precise excision to guarantee a functional new MAC genome. Here, we characterize a pair of paralogous PHD finger proteins involved in DNA elimination. DevPF1, the early-expressed paralog, is present in only some of the gametic and post-zygotic nuclei during meiosis. Both DevPF1 and DevPF2 localize in the new developing MACs, where IES excision occurs. Upon DevPF2 knockdown (KD), long IESs are preferentially retained and late-expressed small RNAs decrease; no length preference for retained IESs was observed in DevPF1-KD and development-specific small RNAs were abolished. The expression of at least two genes from the new MAC with roles in genome reorganization seems to be influenced by DevPF1- and DevPF2-KD. Thus, both PHD fingers are crucial for new MAC genome development, with distinct functions, potentially via regulation of non-coding and coding transcription in the MICs and new MACs.

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Journal
Journal of Cell Science
Published
2024-08-15
DOI
https://doi.org/10.1242/jcs.261979
Primary Topic
Protist diversity and phylogeny
Type
article
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article

Two paralogous PHD finger proteins participate in natural genome editing in Paramecium tetraurelia

Aditi Singh, Estienne C. Swart, Lilia Häußermann
Journal of Cell Science
Protist diversity and phylogeny
article

Two paralogous PHD finger proteins participate in natural genome editing in Paramecium tetraurelia

Aditi Singh, Estienne C. Swart, Lilia Häußermann
article en

Abstract

The unicellular eukaryote Paramecium tetraurelia contains functionally distinct nuclei: germline micronuclei (MICs) and a somatic macronucleus (MAC). During sex, the MIC genome is reorganized into a new MAC genome and the old MAC is lost. Almost 45,000 unique internal eliminated sequences (IESs) distributed throughout the genome require precise excision to guarantee a functional new MAC genome. Here, we characterize a pair of paralogous PHD finger proteins involved in DNA elimination. DevPF1, the early-expressed paralog, is present in only some of the gametic and post-zygotic nuclei during meiosis. Both DevPF1 and DevPF2 localize in the new developing MACs, where IES excision occurs. Upon DevPF2 knockdown (KD), long IESs are preferentially retained and late-expressed small RNAs decrease; no length preference for retained IESs was observed in DevPF1-KD and development-specific small RNAs were abolished. The expression of at least two genes from the new MAC with roles in genome reorganization seems to be influenced by DevPF1- and DevPF2-KD. Thus, both PHD fingers are crucial for new MAC genome development, with distinct functions, potentially via regulation of non-coding and coding transcription in the MICs and new MACs.

Journal of Cell ScienceVol. 137(16)
Max Planck Institute for Biology (DE)
Openalex Percentile: Top 87%
Protist diversity and phylogeny
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Two paralogous PHD finger proteins participate in natural genome editing in <i>Paramecium tetraurelia</i> — Aditi Singh, Estienne C. Swart, et al. · Journal of Cell Science (2024) | TGRS Research Map | TGRS