Evidence map›Paper›PMID 30621145›Full record

ReviewBiology2019

Cyclin C: The Story of a Non-Cycling Cyclin.

Jan Ježek, Daniel G J Smethurst, David C Stieg, Z A C Kiss, Sara E Hanley, Vidyaramanan Ganesan, Kai-Ti Chang, Katrina F Cooper, Randy Strich

Open access · goldAbstract readReview
In one paragraph

Review in Biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Substrates of the MAPK Slt2: Shaping Yeast Cell Integrity.Journal of fungi (Basel, Switzerland) · 2022
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Potential roles of mediator Complex Subunit 13 in Cardiac Diseases.International journal of biological sciences · 2021
    Review
  19. Article
  20. 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

9 authors at 1 institution in 1 country.

Jan JežekDepartment of Molecular Biology, School of Osteopathic Medicine, Rowan University, Stratford, NJ 08084, USA. jezekj6@rowan.edu.ORCID 0000-0003-0295-066X
Daniel G J SmethurstDepartment of Molecular Biology, School of Osteopathic Medicine, Rowan University, Stratford, NJ 08084, USA. smethurstd@rowan.edu.
David C StiegDepartment of Molecular Biology, School of Osteopathic Medicine, Rowan University, Stratford, NJ 08084, USA. stiegdc@rowan.edu.
Z A C KissDepartment of Molecular Biology, School of Osteopathic Medicine, Rowan University, Stratford, NJ 08084, USA. kissz55@rowan.edu.ORCID 0000-0002-1014-0301
Sara E HanleyDepartment of Molecular Biology, School of Osteopathic Medicine, Rowan University, Stratford, NJ 08084, USA. hanleys2@rowan.edu.
Vidyaramanan GanesanDepartment of Molecular Biology, School of Osteopathic Medicine, Rowan University, Stratford, NJ 08084, USA. vidu.biologist@gmail.com.
Kai-Ti ChangDepartment of Molecular Biology, School of Osteopathic Medicine, Rowan University, Stratford, NJ 08084, USA. changk@rowan.edu.
Katrina F CooperDepartment of Molecular Biology, School of Osteopathic Medicine, Rowan University, Stratford, NJ 08084, USA. cooperka@rowan.edu.
Randy StrichDepartment of Molecular Biology, School of Osteopathic Medicine, Rowan University, Stratford, NJ 08084, USA. strichra@rowan.edu.
Rowan University · US

Funding

National Institutes of Health GM R15-113196National Institutes of Health GM RO1-113052
6 · The paper itself

Abstract

The class I cyclin family is a well-studied group of structurally conserved proteins that interact with their associated cyclin-dependent kinases (Cdks) to regulate different stages of cell cycle progression depending on their oscillating expression levels. However, the role of class II cyclins, which primarily act as transcription factors and whose expression remains constant throughout the cell cycle, is less well understood. As a classic example of a transcriptional cyclin, cyclin C forms a regulatory sub-complex with its partner kinase Cdk8 and two accessory subunits Med12 and Med13 called the Cdk8-dependent kinase module (CKM). The CKM reversibly associates with the multi-subunit transcriptional coactivator complex, the Mediator, to modulate RNA polymerase II-dependent transcription. Apart from its transcriptional regulatory function, recent research has revealed a novel signaling role for cyclin C at the mitochondria. Upon oxidative stress, cyclin C leaves the nucleus and directly activates the guanosine 5'-triphosphatase (GTPase) Drp1, or Dnm1 in yeast, to induce mitochondrial fragmentation. Importantly, cyclin C-induced mitochondrial fission was found to increase sensitivity of both mammalian and yeast cells to apoptosis. Here, we review and discuss the biology of cyclin C, focusing mainly on its transcriptional and non-transcriptional roles in tumor promotion or suppression.

Indexed as

cancerCdk8-dependent kinase modulecyclin familyMediatorstress signalingtranscriptional cyclinstumor suppressoryeast

Identifiers

PMID30621145
PMCPMC6466611
OpenAlexW2908302029

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.