Evidence map›Paper›PMID 11157774›Full record

ArticleGenes & development2001

Drosophila stem loop binding protein coordinates accumulation of mature histone mRNA with cell cycle progression.

E Sullivan, C Santiago, E D Parker, Z Dominski, X Yang, D J Lanzotti, T C Ingledue, W F Marzluff, R J Duronio

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing 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

85 citing papers in PubMed, 136 citations in OpenAlex.

  1. Article
  2. SLBP-independent control of maternal histone mRNA.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Cell signaling and epigenetic regulation of nicotine-induced carcinogenesis.Environmental pollution (Barking, Essex : 1987) · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Reduced histone gene copy number disruptsbioRxiv : the preprint server for biology · 2023
    Article
  11. Article
  12. Polyadenylation of canonical histone H3.1 in carcinogenesis.Advances in pharmacology (San Diego, Calif.) · 2023
    Article
  13. Article
  14. Stem-loop binding protein and metal carcinogenesis.Seminars in cancer biology · 2021
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

25 more citing papers are in PubMed but not listed here.

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 at 4 institutions in 4 countries.

E SullivanProgram in Molecular Biology and Biotechnology, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
C Santiago
E D Parker
Z Dominski
X Yang
D J Lanzotti
T C Ingledue
W F Marzluff
R J Duronio
University of North Carolina at Chapel Hill · USInstitute of Molecular Biology and Biophysics · RUUNC Lineberger Comprehensive Cancer CenterUniversity of Puerto Rico System · PR

Funding

HISTONE MRNA REGULATION IN DEVELOPMENTR01GM058921 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DURONIO, ROBERT J, MARZLUFF, WILLIAM F. · 1999 to 2025
$11.6M
GENETIC ANALYSIS OF E2F FUNCTION DURING DEVELOPMENTR01GM057859 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DURONIO, ROBERT J · 1999 to 2012
$3.5M
NIGMS NIH HHS GM57859NIGMS NIH HHS GM58921NIGMS NIH HHS R01 GM057859NIGMS NIH HHS R01 GM058921
6 · The paper itself

Abstract

Replication-associated histone genes encode the only metazoan mRNAs that lack polyA tails, ending instead in a conserved 26-nt sequence that forms a stem-loop. Most of the regulation of mammalian histone mRNA is posttranscriptional and mediated by this unique 3' end. Stem-loop-binding protein (SLBP) binds to the histone mRNA 3' end and is thought to participate in all aspects of histone mRNA metabolism, including cell cycle regulation. To examine SLBP function genetically, we have cloned the gene encoding Drosophila SLBP (dSLBP) by a yeast three-hybrid method and have isolated mutations in dSLBP. dSLBP function is required both zygotically and maternally. Strong dSLBP alleles cause zygotic lethality late in development and result in production of stable histone mRNA that accumulates in nonreplicating cells. These histone mRNAs are cytoplasmic and have polyadenylated 3' ends like other polymerase II transcripts. Hypomorphic dSLBP alleles support zygotic development but cause female sterility. Eggs from these females contain dramatically reduced levels of histone mRNA, and mutant embryos are not able to complete the syncytial embryonic cycles. This is in part because of a failure of chromosome condensation at mitosis that blocks normal anaphase. These data demonstrate that dSLBP is required in vivo for 3' end processing of histone pre-mRNA, and that this is an essential function for development. Moreover, dSLBP-dependent processing plays an important role in coupling histone mRNA production with the cell cycle.

Indexed as

Drosophila ProteinsmRNA Cleavage and Polyadenylation FactorsNuclear ProteinsXenopus ProteinsAmino Acid SequenceAnimalsBase SequenceCell CycleCloning, MolecularDNA, ComplementaryDrosophilaFemaleGenes, InsectHistonesInsect ProteinsMolecular Sequence DataDNA, ComplementaryDrosophila ProteinsHistonesInsect ProteinsmRNA Cleavage and Polyadenylation FactorsNuclear ProteinsRecombinant ProteinsRNA-Binding ProteinsRNA, MessengerSLBP1 protein, XenopusSLBP protein, DrosophilaXenopus Proteins

Identifiers

PMID11157774
PMCPMC312608
OpenAlexW2139631353

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.