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DOI 10.1038/s41467-025-64817-w

Медицинская библиотека · Nature communications · 2025

Multi-layered dosage compensation of the avian Z chromosome by increased transcriptional burst frequency and elevated translational rates.

Papanicolaou Natali, Lentini Antonio, Wettersten Sebastian, Hagemann-Jensen Michael, Krüger Annika, Zhang Jilin, Coucoravas Christos, Petrosian Ioannis, Xin Xian, Ceyhan Ilhan, Rorbach Joanna, Wright Dominic, Reinius Björn

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Аннотация

Sex-chromosome dosage poses a challenge for heterogametic species in maintaining the proper balance of gene products across chromosomes in each sex. While therian mammals (XX/XY system) achieve near-perfect balance of X-chromosome mRNAs through X-upregulation and X-inactivation, birds (ZW/ZZ system) have been found to lack efficient compensation at RNA level, challenging the necessity of resolving major gene-dosage asymmetries in avian cells. Through comprehensive allele-resolved multiome analyses, we examine dosage compensation in female (ZW), male (ZZ), and rare intersex (ZZW) chicken. Our data reveal that females upregulate their single Z chromosome through increased transcriptional burst frequency, mirroring mammalian X upregulation. Z-protein levels are further balanced in females through enhanced translation efficiency. Additionally, we present a global analysis of promoter elements regulating transcriptional burst kinetics in birds, revealing evolutionary conservation of the genomic encoding of burst kinetics between birds and mammals. Our study provides insights into the regulation of avian dosage compensation, and when considering all regulatory layers collectively, an unexpected similarity between avian and mammalian dosage compensation becomes apparent.

Для цитирования: Papanicolaou Natali, Lentini Antonio, Wettersten Sebastian, Hagemann-Jensen Michael, Krüger Annika, Zhang Jilin, Coucoravas Christos, Petrosian Ioannis, Xin Xian, Ceyhan Ilhan, Rorbach Joanna, Wright Dominic, Reinius Björn. Multi-layered dosage compensation of the avian Z chromosome by increased transcriptional burst frequency and elevated translational rates.. Nature communications. 2025. DOI: 10.1038/s41467-025-64817-w.

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