Evidence map›Paper›PMID 20883044›Full record

ArticleJournal of proteome research2010

Oocyte spindle proteomics analysis leading to rescue of chromosome congression defects in cloned embryos.

Zhiming Han, Cheng-Guang Liang, Yong Cheng, Xunbao Duan, Zhisheng Zhong, Santhi Potireddy, Camilo Moncada, Salim Merali, Keith E Latham

Abstract read
In one paragraph

Article in Journal of proteome research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.2field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

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  11. A caffeine fix for human nuclear transfer?Nature biotechnology · 2013
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  14. Review
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  17. Do nuclear envelope and intranuclear proteins reorganize during mitosis to form an elastic, hydrogel-like spindle matrix?Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2011
    Review
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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

9 authors at 1 institution in 1 country.

Zhiming Han *The Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine.
Cheng-Guang Liang *The Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine.
Yong Cheng *The Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine.
Xunbao DuanDepartment of Biochemistry, Temple University School of Medicine.
Zhisheng ZhongThe Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine.
Santhi PotireddyThe Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine.
Camilo MoncadaDepartment of Biochemistry, Temple University School of Medicine.
Salim MeraliDepartment of Biochemistry, Temple University School of Medicine.
Keith E LathamThe Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine.
Temple University · US

Funding

Spindle Formation and Function in Oocytes and Early EmbryosR01HD052788 · NICHD · TEMPLE UNIV OF THE COMMONWEALTH · PI LATHAM, KEITH E · 2006 to 2010
$1.4M
NICHD NIH HHS HD52788NICHD NIH HHS R01 HD052788
6 · The paper itself

Abstract

Embryos produced by somatic cell nuclear transfer (SCNT) display low term developmental potential. This is associated with deficiencies in spindle composition prior to activation and at early mitotic divisions, including failure to assemble certain proteins on the spindle. The protein-deficient spindles are accompanied by chromosome congression defects prior to activation and during the first mitotic divisions of the embryo. The molecular basis for these deficiencies and how they might be avoided are unknown. Proteomic analyses of spindles isolated from normal metaphase II (MII) stage oocytes and SCNT constructs, along with a systematic immunofluorescent survey of known spindle-associated proteins were undertaken. This was the first proteomics study of mammalian oocyte spindles. The study revealed four proteins as being deficient in spindles of SCNT embryos in addition to those previously identified; these were clathrin heavy chain (CLTC), aurora B kinase, dynactin 4, and casein kinase 1 alpha. Due to substantial reduction in CLTC abundance after spindle removal, we undertook functional studies to explore the importance of CLTC in oocyte spindle function and in chromosome congression defects of cloned embryos. Using siRNA knockdown, we demonstrated an essential role for CLTC in chromosome congression during oocyte maturation. We also demonstrated rescue of chromosome congression defects in SCNT embryos at the first mitosis using CLTC mRNA injection. These studies are the first to employ proteomics analyses coupled to functional interventions to rescue a specific molecular defect in cloned embryos.

Indexed as

Cloning, OrganismAnimalsAurora Kinase BAurora KinasesCasein Kinase IChromosome SegregationClathrin Heavy ChainsDynactin ComplexEmbryo, MammalianMiceMice, Inbred StrainsMicrotubule-Associated ProteinsOocytesProteinsProtein Serine-Threonine KinasesProteomicsAurkb protein, mouseAurora Kinase BAurora KinasesCasein Kinase IClathrin Heavy ChainsDynactin ComplexMicrotubule-Associated ProteinsProteinsProtein Serine-Threonine KinasesRNA, Messenger

Identifiers

PMID20883044
PMCPMC4316211
OpenAlexW2044152079

What OpenQuestion holds

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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.