Evidence map›Paper›PMID 31619757›Full record

ArticleScientific reports2019

High-resolution transcriptional profiling of Anopheles gambiae spermatogenesis reveals mechanisms of sex chromosome regulation.

Chrysanthi Taxiarchi, Nace Kranjc, Antonios Kriezis, Kyros Kyrou, Federica Bernardini, Steven Russell, Tony Nolan, Andrea Crisanti, Roberto Galizi

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. A single-nucleus transcriptomic atlas of the adultbioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Engineering drive-selection balance for localized population suppression with neutral dynamics.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Natural and Engineered Sex Ratio Distortion in Insects.Frontiers in ecology and evolution · 2022
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Chrysanthi TaxiarchiDepartment of Life Sciences, Imperial College London, London, UK.
Nace KranjcDepartment of Life Sciences, Imperial College London, London, UK.
Antonios KriezisDepartment of Life Sciences, Imperial College London, London, UK.
Kyros KyrouDepartment of Life Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-4919-2459
Federica BernardiniDepartment of Life Sciences, Imperial College London, London, UK.
Steven RussellDepartment of Genetics, University of Cambridge, Cambridge, UK.
Tony NolanDepartment of Life Sciences, Imperial College London, London, UK.
Andrea CrisantiDepartment of Life Sciences, Imperial College London, London, UK.
Roberto GaliziDepartment of Life Sciences, Imperial College London, London, UK. r.galizi@outlook.com.ORCID http://orcid.org/0000-0003-3134-7480

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although of high priority for the development of genetic tools to control malaria-transmitting mosquitoes, only a few germline-specific regulatory regions have been characterised to date and the presence of global regulatory mechanisms, such as dosage compensation and meiotic sex chromosome inactivation (MSCI), are mostly assumed from transcriptomic analyses of reproductive tissues or whole gonads. In such studies, samples include a significant portion of somatic tissues inevitably complicating the reconstruction of a defined transcriptional map of gametogenesis. By exploiting recent advances in transgenic technologies and gene editing tools, combined with fluorescence-activated cell sorting and RNA sequencing, we have separated four distinct cell lineages from the Anopheles gambiae male gonads: premeiotic, meiotic (primary and secondary spermatocytes) and postmeiotic. By comparing the overall expression levels of X-linked and autosomal genes across the four populations, we revealed a striking transcriptional repression of the X chromosome coincident with the meiotic phase, classifiable as MSCI, and highlighted genes that may evade silencing. In addition, chromosome-wide median expression ratios of the premeiotic population confirmed the absence of dosage compensation in the male germline. Applying differential expression analysis, we highlighted genes and transcript isoforms enriched at specific timepoints and reconstructed the expression dynamics of the main biological processes regulating the key stages of sperm development and maturation. We generated the first transcriptomic atlas of A. gambiae spermatogenesis that will expand the available toolbox for the genetic engineering of vector control technologies. We also describe an innovative and multidimensional approach to isolate specific cell lineages that can be used for the targeted analysis of other A. gambiae organs or transferred to other medically relevant species and model organisms.

Indexed as

AnimalsAnimals, Genetically ModifiedAnophelesGene Expression Regulation, DevelopmentalGenes, X-LinkedMalariaMaleMosquito ControlMosquito VectorsSpermatogenesisTestisTranscriptomeX Chromosome

Identifiers

PMID31619757
PMCPMC6795909

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.