Evidence map›Paper›PMID 10207114›Full record

ArticleMolecular and cellular biology1999

Sequence-independent assembly of spermatid mRNAs into messenger ribonucleoprotein particles.

E E Schmidt, E S Hanson, M R Capecchi

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  7. Illegitimate Cre-dependent chromosome rearrangements in transgenic mouse spermatids.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  8. 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

3 authors at 2 institutions in 1 country.

E E SchmidtHoward Hughes Medical Institute, Eccles Institute of Human Genetics, University of Utah, Salt Lake City, Utah 84112, USA. eschmidt@howard.genetics.utah.edu
E S Hanson
M R Capecchi
Howard Hughes Medical Institute · USUniversity of Utah · US

Funding

RESEARCH TRAINING IN HEMATOLOGYT32DK007115 · NIDDK · UNIVERSITY OF UTAH · PI LEIBOLD, ELIZABETH ANN, PRCHAL, JOSEF T · 1986 to 2020
$8.4M
NIDDK NIH HHS T32 DK007115NIDDK NIH HHS T32 DK07115
6 · The paper itself

Abstract

During mammalian spermatogenesis, meiosis is followed by a brief period of high transcriptional activity. At this time a large amount of mRNA is stored as messenger ribonucleoprotein (mRNP) particles. All subsequent processes of sperm maturation occur in the complete absence of transcription, primarily using proteins which are newly synthesized from these stored mRNAs. By expressing transgene mRNAs in the early haploid spermatids of mice, we have investigated the sequence requirements for determining whether specific mRNAs in these cells will be stored as mRNP particles or be assembled into polysomes. The results suggest that mRNAs which are transcribed in spermatids are assembled into mRNP particles by a mechanism that acts independently of mRNA sequence. Our findings reveal a fundamental similarity between the mechanisms of translational control used in spermatogenesis and oogenesis.

Indexed as

AnimalsCell LineFlow CytometryGene Expression RegulationGlyceraldehyde-3-Phosphate DehydrogenasesMaleMiceMice, TransgenicMicroscopy, FluorescenceOocytesPolyribosomesProtaminesProtein BiosynthesisRibonucleoproteinsRNA, MessengerSpermatidsGlyceraldehyde-3-Phosphate DehydrogenasesPrm1 protein, mouseProtaminesRibonucleoproteinsRNA, Messenger

Identifiers

PMID10207114
PMCPMC84248
OpenAlexW2118854491

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.