Evidence map›Paper›PMID 28318374›Full record

ArticleCell cycle (Georgetown, Tex.)2017

Identification and characterization of the BmCyclin L1-BmCDK11A/B complex in relation to cell cycle regulation.

Tai-Hang Liu, Yun-Fei Wu, Xiao-Long Dong, Cai-Xia Pan, Guo-Yu Du, Ji-Gui Yang, Wei Wang, Xi-Yan Bao, Peng Chen, Min-Hui Pan and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

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  7. Whole-exome sequencing of familial esophageal squamous cell carcinoma identified rare pathogenic variants in new predisposition genes.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
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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

11 authors at 2 institutions in 1 country.

Tai-Hang Liua State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
Yun-Fei Wua State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
Xiao-Long Donga State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
Cai-Xia Pana State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
Guo-Yu Dua State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
Ji-Gui Yanga State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
Wei Wanga State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
Xi-Yan Baoa State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
Peng Chena State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
Min-Hui Pana State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
Cheng Lua State Key Laboratory of Silkworm Genome Biology , Southwest University , Chongqing , China.
State Key Laboratory of Silkworm Genomic BiologySouthwest University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclin proteins are the key regulatory and activity partner of cyclin-dependent kinases (CDKs), which play pivotal regulatory roles in cell cycle progression. In the present study, we identified a Cyclin L1 and 2 CDK11 2 CDK11 splice variants, CDK11A and CDK11B, from silkworm, Bombyx mori. We determined that both Cyclin L1 and CDK11A/B are nuclear proteins, and further investigations were conducted to elucidate their spatiofunctional features. Cyclin L1 forms a complex with CDK11A/B and were co-localized to the nucleus. Moreover, the dimerization of CDK11A and CDK11B and the effects of Cyclin L1 and CDK11A/B on cell cycle regulation were also investigated. Using overexpression or RNA interference experiments, we demonstrated that the abnormal expression of Cyclin L1 and CDK11A/B leads to cell cycle arrest and cell proliferation suppression. Together, these findings indicate that CDK11A/B interacts with Cyclin L1 to regulate the cell cycle.

Indexed as

Cell CycleAmino Acid SequenceAnimalsBombyxCell Cycle CheckpointsCell ProliferationCloning, MolecularCyclin-Dependent KinasesCyclinsInsect ProteinsNuclear Localization SignalsPhylogenyProtein MultimerizationCyclin-Dependent KinasesCyclinsInsect ProteinsNuclear Localization SignalsBombyx moriCDK11cell cyclecyclin L1NLS

Identifiers

PMID28318374
PMCPMC5444353
OpenAlexW2599322127

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.