Evidence map›Paper›PMID 21427144›Full record

ArticleDevelopment (Cambridge, England)2011

The poly(A) polymerase GLD2 is required for spermatogenesis in Drosophila melanogaster.

Caroline V Sartain, Jun Cui, Richard P Meisel, Mariana F Wolfner

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
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

33 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Terminal nucleotidyltransferaseRNA (New York, N.Y.) · 2025
    Article
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  6. Article
  7. Article
  8. Review
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  11. Review
  12. Article
  13. Review
  14. Terminal nucleotidyl transferases (TENTs) in mammalian RNA metabolism.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
  15. 5' and 3' modifications controlling RNA degradation: from safeguards to executioners.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Article
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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

4 authors at 1 institution in 1 country.

Caroline V SartainDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.
Jun Cui
Richard P Meisel
Mariana F Wolfner
Cornell University · US

Funding

PREDOCTORAL TRAINING IN GENETICS AND DEVELOPMENTT32GM007617 · NIGMS · CORNELL UNIVERSITY ITHACA · PI BARBASH, DANIEL A · 1985 to 2021
$5.5M
MOLECULAR GENETICS OF PRONUCLEAR FUSION IN DROSOPHILAR01GM044659 · NIGMS · CORNELL UNIVERSITY ITHACA · PI WOLFNER, MARIANA FEDERICA · 1991 to 2010
$2.6M
Gene Expression, Duplicated Genes, and Sex Bias in DrosophilaF32GM087611 · NIGMS · CORNELL UNIVERSITY · PI MEISEL, RICHARD P. · 2008 to 2010
$143k
NIGMS NIH HHS F32-GM08611NIGMS NIH HHS F32 GM087611NIGMS NIH HHS R01 GM044659NIGMS NIH HHS R01-GM44659NIGMS NIH HHS T32 GM007617NIGMS NIH HHS T32 GM07617
6 · The paper itself

Abstract

The DNA of a developing sperm is normally inaccessible for transcription for part of spermatogenesis in many animals. In Drosophila melanogaster, many transcripts needed for late spermatid differentiation are synthesized in pre-meiotic spermatocytes, but are not translated until later stages. Thus, post-transcriptional control mechanisms are required to decouple transcription and translation during spermatogenesis. In the female germline, developing germ cells accomplish similar decoupling through poly(A) tail alterations to ensure that dormant transcripts are not prematurely translated: a transcript with a short poly(A) tail will remain untranslated, whereas elongating the poly(A) tail permits protein production. In Drosophila, the ovary-expressed cytoplasmic poly(A) polymerase WISPY is responsible for stage-specific poly(A) tail extension in the female germline. Here, we examine the possibility that a recently derived testis-expressed WISPY paralog, GLD2, plays a similar role in the Drosophila male germline. We show that knockdown of Gld2 transcripts causes male sterility, as GLD2-deficient males do not produce mature sperm. Spermatogenesis up to and including meiosis appears normal in the absence of GLD2, but post-meiotic spermatid development rapidly becomes abnormal. Nuclear bundling and F-actin assembly are defective in GLD2 knockdown testes and nuclei fail to undergo chromatin reorganization in elongated spermatids. GLD2 also affects the incorporation of protamines and the stability of dynamin and transition protein transcripts. Our results indicate that GLD2 is an important regulator of late spermatogenesis and is the first example of a Gld-2 family member that plays a significant role specifically in male gametogenesis.

Indexed as

AnimalsBlotting, WesternDrosophila melanogasterFemaleMaleMicroscopy, FluorescenceMicroscopy, Phase-ContrastModels, BiologicalPolynucleotide AdenylyltransferaseReverse Transcriptase Polymerase Chain ReactionSpermatogenesisTestisTwo-Hybrid System TechniquesPolynucleotide Adenylyltransferase

Identifiers

PMID21427144
PMCPMC3062429
OpenAlexW2121194489

What OpenQuestion holds

Textmetadata
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.