Evidence map›Paper›PMID 41833836›Full record

ArticleDevelopmental biology2026

Discrete 3' UTR sequence motifs regulate nanos RNA enrichment in Drosophila germ granules.

Kira Mitchel, Elizabeth R Gavis

Abstract read
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Article in Developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Kira MitchelDepartment of Molecular Biology, Princeton University, Princeton, NJ, 08544, USA.
Elizabeth R GavisDepartment of Molecular Biology, Princeton University, Princeton, NJ, 08544, USA. Electronic address: gavis@princeton.edu.

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007388 · NIGMS · PRINCETON UNIVERSITY · PI CRISTEA, ILEANA M. · 1985 to 2022
$27.4M
Mechanisms of mRNA localization and translational control in Drosophila developmentR35GM126967 · NIGMS · PRINCETON UNIVERSITY · PI ELIZABETH R GAVIS · 2018 to 2026
$5.9M
NIGMS NIH HHS R35 GM126967NIGMS NIH HHS T32 GM007388
6 · The paper itself

Abstract

Germ granules are ribonucleoprotein condensates that concentrate key maternal mRNAs needed for germ cell development. In Drosophila, nanos mRNA is selectively enriched in germ granules but the specific cis-acting elements mediating this process remain poorly defined. Here, we identify discrete sequence motifs in the nanos 3' UTR that regulate nanos enrichment specifically by promoting the growth of homotypic nanos mRNA clusters within granules, without affecting the initial targeting of nanos to germ granules. These sequence motifs are binding sites for the hnRNP M homolog Rumpelstiltskin (Rump) and mutation of Rump binding sites or Rump attenuates nanos homotypic cluster growth, reducing the amount of nanos inherited by germ cells. Consequently, germ cells exhibit defective migration to the gonad. Together, our findings reveal how small repeated sequence motifs and cognate RNA-binding proteins can tune enrichment of germ granule mRNAs by driving self-assembly into large RNA clusters. This strategy ensures sufficient inheritance of mRNAs to support germ cell development and may represent a general mechanism by which ribonucleoprotein condensates regulate transcript dosage.

Indexed as

3' Untranslated RegionsDrosophila melanogasterDrosophila ProteinsGerm CellsRNA-Binding ProteinsAnimalsBase SequenceBinding SitesCytoplasmic GranulesHeterogeneous-Nuclear RibonucleoproteinsNucleotide MotifsRNA, Messenger3' Untranslated RegionsDrosophila ProteinsHeterogeneous-Nuclear Ribonucleoproteinsnos protein, DrosophilaRNA-Binding ProteinsRNA, Messenger

Identifiers

PMID41833836
PMCPMC13151403

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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.