Evidence map›Paper›PMID 9499407›Full record

ArticleGenes & development1998

Cell cycle control of chorion gene amplification.

B R Calvi, M A Lilly, A C Spradling

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers.

0numbers the graph read from it
0cells of the map it votes in
134citing 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

134 citing papers in PubMed, 252 citations in OpenAlex.

  1. Article
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  3. RNA Sequencing in AdultbioRxiv : the preprint server for biology · 2026
    Article
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  7. Article
  8. Cell-cycle-regulated transcriptional pausing ofMolecular biology of the cell · 2025
    Article
  9. Article
  10. Cell cycle-regulated transcriptional pausing ofbioRxiv : the preprint server for biology · 2024
    Article
  11. Article
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  13. Article
  14. Finishing the egg.Genetics · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Noncanonical function of Capicua as a growth termination signal inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article

74 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

3 authors at 2 institutions in 1 country.

B R CalviHoward Hughes Medical Institute Research Laboratories, Carnegie Institution of Washington, Baltimore, Maryland 21210, USA.
M A Lilly
A C Spradling
Carnegie Observatories · USHoward Hughes Medical Institute · US

Funding

NORMAL AND MUTANT CHORION GENES OF DROSOPHILAR37GM027875 · NIGMS · CARNEGIE INSTITUTION OF WASHINGTON, D.C. · PI SPRADLING, ALLAN C · 1993 to 2003
$661k
NORMAL AND MUTANT CHORION GENES OF DROSPHILAR01GM027875 · NIGMS · CARNEGIE INSTITUTION OF WASHINGTON, DC · PI SPRADLING, ALLAN C · 1985 to 1992
–
Howard Hughes Medical InstituteNIGMS NIH HHS GM27875
6 · The paper itself

Abstract

Over-replication of two clusters of chorion genes in Drosophila ovarian follicle cells is essential for rapid eggshell biosynthesis. The relationship of this amplification to the follicle cell cycles has remained unclear. To investigate the regulation of amplification, we developed a technique to detect amplifying chorion genes in individual follicle cells using BrdU incorporation and FISH. Amplification occurs in two developmental phases. One of the gene clusters begins to amplify periodically during S phases of follicle cell endocycles. Subsequently, after endocycles have ceased, both clusters amplify continuously during the remainder of oogenesis. In contrast to the early phase, late amplification commences synchronously among follicle cells. The pattern of Cyclin E expression mirrors these two phases. We present evidence that Cyclin E is required positively for amplification. We suggest that Cyclin E also acts negatively to inhibit refiring of most origins within a cycle, and that specific factors at chorion origins allow them to escape this negative rereplication control. Our findings suggest that chorion amplification is a model for understanding metazoan replicons and the controls that restrict replication to once per cell cycle.

Indexed as

Gene AmplificationAnimalsCell CycleChorionCyclin EDNA ReplicationDrosophilaEmbryo, NonmammalianFemaleOvarian FollicleCyclin E

Identifiers

PMID9499407
PMCPMC316579
OpenAlexW2108450183

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.