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Randomly incorporated genomic 6mA delays zygotic transcription initiation

View ORCID ProfileFebrimarsa, View ORCID ProfileSebastian G Gornik, View ORCID ProfileSofia N Barreira, View ORCID ProfileMiguel Salinas-Saavedra, View ORCID ProfileChristine E Schnitzler, View ORCID ProfileAndreas D Baxevanis, View ORCID ProfileUri Frank
doi: https://doi.org/10.1101/2022.10.27.514014
Febrimarsa
1Centre for Chromosome Biology, School of Biological and Chemical Sciences, University of Galway, Galway, Republic of Ireland
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Sebastian G Gornik
1Centre for Chromosome Biology, School of Biological and Chemical Sciences, University of Galway, Galway, Republic of Ireland
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Sofia N Barreira
2Computational and Statistical Genomics Branch, Division of Intramural Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA
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Miguel Salinas-Saavedra
1Centre for Chromosome Biology, School of Biological and Chemical Sciences, University of Galway, Galway, Republic of Ireland
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Christine E Schnitzler
3Whitney Laboratory for Marine Bioscience, University of Florida, St. Augustine, FL 32080, USA
4Department of Biology, University of Florida, Gainesville, FL 32611, USA
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Andreas D Baxevanis
2Computational and Statistical Genomics Branch, Division of Intramural Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA
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Uri Frank
1Centre for Chromosome Biology, School of Biological and Chemical Sciences, University of Galway, Galway, Republic of Ireland
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  • For correspondence: uri.frank@nuigalway.ie
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SUMMARY

N6-methyldeoxyadenosine (6mA) is a chemical alteration of DNA, observed across all realms of life. The functions of 6mA are well understood in bacteria but its roles in animal genomes have been controversial. We show that 6mA randomly accumulates in early embryos of the cnidarian Hydractinia symbiolongicarpus, with a peak at the 16-cell stage followed by clearance to background levels two cell cycles later, at the 64-cell stage – the embryonic stage at which zygotic genome activation occurs in this animal. Knocking down Alkbh1, a putative initiator of animal 6mA clearance, resulted in higher levels of 6mA at the 64-cell stage and a delay in the commencement of zygotic transcription. Our data are consistent with 6mA originating from recycled nucleotides of degraded m6A-marked maternal RNA post-fertilization. Therefore, while 6mA does not function as an epigenetic mark in Hydractinia, its random incorporation into the early embryonic genome inhibits transcription. Alkbh1 functions as a genomic 6mA ‘cleaner’, facilitating timely zygotic genome activation. Given the random nature of genomic 6mA accumulation and its ability to interfere with gene expression, defects in 6mA clearance may represent a hitherto unknown cause of various pathologies.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted October 27, 2022.
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Randomly incorporated genomic 6mA delays zygotic transcription initiation
Febrimarsa, Sebastian G Gornik, Sofia N Barreira, Miguel Salinas-Saavedra, Christine E Schnitzler, Andreas D Baxevanis, Uri Frank
bioRxiv 2022.10.27.514014; doi: https://doi.org/10.1101/2022.10.27.514014
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Randomly incorporated genomic 6mA delays zygotic transcription initiation
Febrimarsa, Sebastian G Gornik, Sofia N Barreira, Miguel Salinas-Saavedra, Christine E Schnitzler, Andreas D Baxevanis, Uri Frank
bioRxiv 2022.10.27.514014; doi: https://doi.org/10.1101/2022.10.27.514014

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