Abstract

Dosage compensation equalizes X-linked expression between XY males and XX females. In male fruit flies, expression levels of the X-chromosome are increased approximately two-fold to compensate for their single X chromosome. In testis, dosage compensation is thought to cease during meiosis; however, the timing and degree of the resulting transcriptional suppression is difficult to separate from global meiotic downregulation of each chromosome. To address this, we analyzed testis single-cell RNA-sequencing (scRNA-seq) data from two Drosophila melanogaster strains. We found evidence that the X chromosome is equally transcriptionally active as autosomes in somatic and pre-meiotic cells, and less transcriptionally active than autosomes in meiotic and post-meiotic cells. In cells experiencing dosage compensation, close proximity to MSL (male-specific lethal) chromatin entry sites (CES) correlates with increased X chromosome transcription. We found low or undetectable levels of germline expression of most msl genes, mle, roX1 and roX2 via scRNA-seq and RNA-FISH, and no evidence of germline nuclear roX1/2 localization. Our results suggest that, although dosage compensation occurs in somatic and pre-meiotic germ cells in Drosophila testis, there might be non-canonical factors involved in the dosage compensation mechanism. The single-cell expression patterns and enrichment statistics of detected genes can be explored interactively in our database: https://zhao.labapps.rockefeller.edu/gene-expr/.

Highlights

  • In a wide variety of sexually reproducing animals, males and females have different numbers of X chromosomes

  • Using single-cell RNA-seq data, we found that certain germ cell types in the Drosophila testis show X chromosome expression similar to that of the autosomes, implying dosage compensation activity

  • We found evidence that genes near a chromatin

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Summary

Introduction

In a wide variety of sexually reproducing animals, males and females have different numbers of X chromosomes. For many sexually reproducing animals, transcription is adjusted to compensate for differing numbers of sex chromosomes, a phenomenon referred to as dosage compensation [2,3]. Strategies for this process vary dramatically across the animal kingdom, some to increase chromosome X transcription in males, others to randomly inactivate one X or to partially suppress both X chromosomes in females [4,5,6,7,8]. The spatial and temporal patterns of dosage compensation are key to understanding gene expression regulation and its roles in development. ScRNA-seq has been successfully used to study dosage compensation during development [9], but has not yet been applied to adult spermatogenesis

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