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Single-cell RNA-sequencing reveals pre-meiotic X-chromosome dosage compensation in Drosophila testis

TLDR
Zhang et al. as mentioned in this paper analyzed testis single-cell RNA-sequencing (scRNA-seq) data from two Drosophila melanogaster strains and found evidence that the X-chromosome is equally transcriptionally active as autosomes in somatic and pre-meiotic cells, and less transcriptionally inactive than auto-somes in meiotic and post-MEiotic cells.
Abstract
Dosage compensation (DC) is a mechanism by which X chromosome transcription is equalized in the somatic cells of both males and females In male fruit flies, expression levels of the X-chromosome are increased 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 level of germline expression of most msl genes, mle, roX1 and roX2 via sequencing or RNA-FISH, and no evidence of germline nuclear roX1/2 localization Our results suggest that, although DC occurs in somatic and premeiotic germ cells in Drosophila testis, there might be non-canonical factors involved in the dosage compensation The single-cell expression patterns and enrichment statistics of detected genes can be explored interactively in our database: https://zhaolabappsrockefelleredu/gene-expr/

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Dynamic regulation of ribosome levels and translation during development.

TL;DR: In this paper , the ability of ribosomes to translate mRNAs into proteins is the basis of all life and they are essential for cell viability, while reduction in levels of the ribosome homeostasis can affect cell fate and developmental transitions in a tissue specific manner.
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A Primer for Single-Cell Sequencing in Non-Model Organisms

TL;DR: This primer describes a general workflow for single-cell sequencing studies and considerations for using non-model organisms (limited to multicellular animals) to allow for a deeper understanding of the mechanisms between genotype and phenotype and the basis for biological variation.
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The Regulation of Germline Sex Determination in Drosophila by Sex lethal

TL;DR: This review will focus on Sxl in the germline, how it is activated specifically in female germ cells, and how it regulates germline sex determination and sexual development.
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Expansion and loss of sperm nuclear basic protein genes in Drosophila correspond with genetic conflicts between sex chromosomes

TL;DR: This paper used a phylogenomic approach to investigate SNBP diversification in Drosophila species and found 19 independent SNBP gene amplification events that occurred preferentially on sex chromosomes.
References
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Spatial reconstruction of single-cell gene expression data

TL;DR: Seurat is a computational strategy to infer cellular localization by integrating single-cell RNA-seq data with in situ RNA patterns, and correctly localizes rare subpopulations, accurately mapping both spatially restricted and scattered groups.
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Interplay between NS3 protease and human La protein regulates translation-replication switch of Hepatitis C virus

TL;DR: It is demonstrated that the NS3 protease (NS3pro) domain alone can specifically bind to HCV-IRES RNA, predominantly in the SLIV region, and that this binding reduces translation in favor of RNA replication.
Journal ArticleDOI

FlyBase 2.0: the next generation.

TL;DR: These major new features and functionalities of the FlyBase 2.0 site are described and how they support the use of Drosophila as a model organism for biological discovery and translational research are described.
Journal ArticleDOI

Meiotic sex chromosome inactivation

James M. A. Turner
- 15 May 2007 - 
TL;DR: This work has established sex chromosome asynapsis as the primary trigger of MSCI, and it is now clear that it is maintained, although not completely, well beyond meiosis and into sperm development.
Journal ArticleDOI

Cellular Source and Mechanisms of High Transcriptome Complexity in the Mammalian Testis

TL;DR: It is shown that transcription of the genome is substantially more widespread in the testis than in other organs across representative mammals, and it is revealed that meiotic spermatocytes and especially postmeiotic round sperMatids have remarkably diverse transcriptomes, which explains the high transcriptome complexity of the testes as a whole.
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