Dataset Information

The sex-specific factor SOA establishes X chromosome dosage compensation in Anopheles mosquitos

ABSTRACT: The Anopheles mosquito is one of thousands of species in which sex differences play a central role in their biology, as only females need a blood meal in order to produce eggs. Sex differentiation is regulated by sex chromosomes, but their presence creates a dosage imbalance between males (XY) and females (XX). Dosage compensation (DC) can re-equilibrate the expression of sex-chromosomal genes, but because the molecular mechanisms providing DC have only been studied in a few model organisms, key questions about its evolutionary diversity and functional necessity remain unresolved. Here, we reveal the DC pathway in the malaria mosquito Anopheles gambiae. We identified SOA, a previously uncharacterized gene, whose expression is sufficient to induce a global upregulation of X-linked genes. Sex-specific alternative splicing prevents the production of a functional SOA protein in females. The male SOA isoform encodes a DNA-binding protein that recognizes the promoters of X chromosomal genes through a CA repeat sequence. Male mosquitos lacking SOA exhibit a chromosome-wide downregulation of the X, which is compatible with viability, but causes a developmental delay. Thus, our molecular analysis of the first DC master regulator in a non-model organism elucidates the evolutionary steps leading to the establishment of a chromosome-specific fine-tuning mechanism.

INSTRUMENT(S): Q Exactive Plus

ORGANISM(S): Anopheles Gambiae (african Malaria Mosquito)

SUBMITTER: F Butter

LAB HEAD: Falk Buttter

PROVIDER: PXD042353 | Pride | 2023-07-13

REPOSITORIES: Pride

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Dataset's files

Source:

			Action	DRS
	20220619_QEP2_FBU_FB_collabCKV_IggIP_male_600_1.raw	Raw
	20220619_QEP2_FBU_FB_collabCKV_IggIP_male_600_1_20220620143343.raw	Raw
	20220619_QEP2_FBU_FB_collabCKV_IggIP_male_600_1_20220621000318.raw	Raw
	20220619_QEP2_FBU_FB_collabCKV_IggIP_male_600_1_20220621093246.raw	Raw
	20220619_QEP2_FBU_FB_collabCKV_SoaIP_male_600_1.raw	Raw

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Publications

The sex-specific factor SOA controls dosage compensation in Anopheles mosquitoes.

Kalita Agata Izabela AI Marois Eric E Kozielska Magdalena M Weissing Franz J FJ Jaouen Etienne E Möckel Martin M MM Rühle Frank F Butter Falk F Basilicata M Felicia MF Keller Valsecchi Claudia Isabelle CI

Nature 20230928 7985

The Anopheles mosquito is one of thousands of species in which sex differences play a central part in their biology, as only females need a blood meal to produce eggs. Sex differentiation is regulated by sex chromosomes, but their presence creates a dosage imbalance between males (XY) and females (XX). Dosage compensation (DC) can re-equilibrate the expression of sex chromosomal genes. However, because DC mechanisms have only been fully characterized in a few model organisms, key questions about ...[more]

PMID: 37769784

Similar Datasets

Project description:In many species, males and females display differences in their physiology that are not limited to the gonads. Sex differences in adult insects can comprise body size and feeding behaviour, as only female, but not male mosquitoes are blood-feeding in order to produce eggs. This is relevant since the malaria-causing parasite Plasmodium is transmitted by a female mosquito through a previous blood meal from an infected individual. The initiation of sex-specific developmental programs can be often linked to heteromorphic sex chromosomes (XX/XY in Anopheles). In males, the X-linked genes are only present in a single copy. To counteract this hemizygosity, Anopheles, like other species, exhibits dosage compensation (DC). Anopheles DC manifests by upregulation of the single male X ensuring the equal expression of sex-chromosomal genes between males and females. To date, the sex-specific differences at the transcriptome level related to the X/Y chromosomes and DC have been characterized at post-embryonic stages. Their onset during embryogenesis, especially during the early stages where the embryo switches from the maternal to the zygotic transcriptome, is largely uncharacterized to date. Here, we generate a sex-specific transcriptome atlas across Anopheles embryogenesis ending at the first larval stage. Along with the transition from the maternal to the zygotic transcriptome, many transcripts switch isoform, where the 3’ untranslated regions (UTR) of zygotic transcripts are significantly extended compared to their maternal counterpart. We also identify stage- and sex-specific splicing events. Comparing male and female embryos, we identify 120 sexually dimorphic protein coding genes and non-coding RNAs, indicating that sexually dimorphic gene expression is not widespread during embryogenesis. Furthermore, the imbalance of X-linked genes between males and females after zygotic genome activation is corrected shortly after, where the majority of genes exhibit DC around 9 hours of embryogenesis with further fine-tuning later in development. Our atlas provides a framework to explore sex differences in development and evolution and thereby, enables future functional analyses of sex-specific expression patterns and isoform usage.