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225: VRK-1 and BAF-1 release meiotic chromosomes

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Manage episode 523740926 series 3682575
Content provided by [email protected] (Gustavo Barra) and Gustavo Barra. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by [email protected] (Gustavo Barra) and Gustavo Barra or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.

️ Episode 225: VRK-1 and BAF-1 release meiotic chromosomes

In this episode of PaperCast Base by Base, we explore VRK-1 phosphorylates BAF-1 to remove chromatin from the nuclear periphery during early meiotic prophase in C. elegans, and failure of this step impairs pairing and synapsis and generates heritable genome lesions

Study Highlights:
The authors used an auxin-inducible VRK-1 depletion system and genetic perturbations to show that VRK-1 phosphorylates BAF-1 (Ser4) to release chromatin–nuclear periphery contacts during leptotene–zygotene. VRK-1 loss or a BAF-1 Ser4 phospho-mutant increases chromatin tethering at the nuclear envelope, delays homolog pairing, slows and disrupts synaptonemal complex assembly, and elevates apoptosis. VRK-1 depletion produces oocytes with increased DAPI bodies, intrachromosomal bridges and fragmentation that depend on SPO-11 and MSH-5, while baf-1 RNAi rescues overtethering phenotypes. Transient VRK-1 loss during the chromosome movement window yields offspring with an increased burden of deletions and duplications detected by long-read sequencing, implicating VRK-1–BAF-1 in preserving genome integrity

Conclusion:
Timed VRK-1–mediated phosphorylation of BAF-1 is required to detach chromatin from the nuclear periphery during meiotic chromosome movements to ensure correct pairing, synapsis, and genome stability

Music:
Enjoy the music based on this article at the end of the episode.

Reference:
Paouneskou D., Baudrimont A., Elkrewi M., Kölbl C., Tiemann-Boege I., Vicoso B., Jantsch V. BAF-1–VRK-1 mediated release of meiotic chromosomes from the nuclear periphery is important for genome integrity. Nature Communications. 2025;16:10446. https://doi.org/10.1038/s41467-025-65420-9

License:
This episode is based on an open-access article published under the Creative Commons Attribution 4.0 International License (CC BY 4.0) – https://creativecommons.org/licenses/by/4.0/

Support:
Base by Base – Stripe donations: https://donate.stripe.com/7sY4gz71B2sN3RWac5gEg00

Official website https://basebybase.com

Castos player https://basebybase.castos.com

On PaperCast Base by Base you’ll discover the latest in genomics, functional genomics, structural genomics, and proteomics.

  continue reading

228 episodes

Artwork
iconShare
 
Manage episode 523740926 series 3682575
Content provided by [email protected] (Gustavo Barra) and Gustavo Barra. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by [email protected] (Gustavo Barra) and Gustavo Barra or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.

️ Episode 225: VRK-1 and BAF-1 release meiotic chromosomes

In this episode of PaperCast Base by Base, we explore VRK-1 phosphorylates BAF-1 to remove chromatin from the nuclear periphery during early meiotic prophase in C. elegans, and failure of this step impairs pairing and synapsis and generates heritable genome lesions

Study Highlights:
The authors used an auxin-inducible VRK-1 depletion system and genetic perturbations to show that VRK-1 phosphorylates BAF-1 (Ser4) to release chromatin–nuclear periphery contacts during leptotene–zygotene. VRK-1 loss or a BAF-1 Ser4 phospho-mutant increases chromatin tethering at the nuclear envelope, delays homolog pairing, slows and disrupts synaptonemal complex assembly, and elevates apoptosis. VRK-1 depletion produces oocytes with increased DAPI bodies, intrachromosomal bridges and fragmentation that depend on SPO-11 and MSH-5, while baf-1 RNAi rescues overtethering phenotypes. Transient VRK-1 loss during the chromosome movement window yields offspring with an increased burden of deletions and duplications detected by long-read sequencing, implicating VRK-1–BAF-1 in preserving genome integrity

Conclusion:
Timed VRK-1–mediated phosphorylation of BAF-1 is required to detach chromatin from the nuclear periphery during meiotic chromosome movements to ensure correct pairing, synapsis, and genome stability

Music:
Enjoy the music based on this article at the end of the episode.

Reference:
Paouneskou D., Baudrimont A., Elkrewi M., Kölbl C., Tiemann-Boege I., Vicoso B., Jantsch V. BAF-1–VRK-1 mediated release of meiotic chromosomes from the nuclear periphery is important for genome integrity. Nature Communications. 2025;16:10446. https://doi.org/10.1038/s41467-025-65420-9

License:
This episode is based on an open-access article published under the Creative Commons Attribution 4.0 International License (CC BY 4.0) – https://creativecommons.org/licenses/by/4.0/

Support:
Base by Base – Stripe donations: https://donate.stripe.com/7sY4gz71B2sN3RWac5gEg00

Official website https://basebybase.com

Castos player https://basebybase.castos.com

On PaperCast Base by Base you’ll discover the latest in genomics, functional genomics, structural genomics, and proteomics.

  continue reading

228 episodes

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