Evidence map›Paper›PMID 22184006›Full record

ArticleCell research2012

Molecular insights into the heterogeneity of telomere reprogramming in induced pluripotent stem cells.

Fang Wang, Yu Yin, Xiaoying Ye, Kai Liu, Haiying Zhu, Lingling Wang, Maria Chiourea, Maja Okuka, Guangzhen Ji, Jiameng Dan and 9 more

Abstract read
In one paragraph

Article in Cell research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

  1. Article
  2. Cellular senescence and aging: molecular mechanisms and convergent pathways.Cellular and molecular life sciences : CMLS · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Tumorigenicity risk of iPSCsPrecision clinical medicine · 2022
    Review
  13. Article
  14. Article
  15. Accelerated neuronal agingFrontiers in aging neuroscience · 2022
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  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

19 authors.

Fang WangCollege of Life Sciences, Nankai University, Tianjin 300071, China.
Yu Yin
Xiaoying Ye
Kai Liu
Haiying Zhu
Lingling Wang
Maria Chiourea
Maja Okuka
Guangzhen Ji
Jiameng Dan
Bingfeng Zuo
Minshu Li
Qian Zhang
Na Liu
Lingyi Chen
Xinghua Pan
Sarantis Gagos
David L Keefe
Lin Liu

Funding

HOX cluster intergenic non-coding RNAs in myeloid differentiation and functionR01DK054369 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI NEWBURGER, PETER E, WEISSMAN, SHERMAN MORTON · 1999 to 2013
$7.2M
NIDDK NIH HHS 2 R01 DK054369NIDDK NIH HHS R01 DK054369
6 · The paper itself

Abstract

Rejuvenation of telomeres with various lengths has been found in induced pluripotent stem cells (iPSCs). Mechanisms of telomere length regulation during induction and proliferation of iPSCs remain elusive. We show that telomere dynamics are variable in mouse iPSCs during reprogramming and passage, and suggest that these differences likely result from multiple potential factors, including the telomerase machinery, telomerase-independent mechanisms and clonal influences including reexpression of exogenous reprogramming factors. Using a genetic model of telomerase-deficient (Terc(-/-) and Terc(+/-)) cells for derivation and passages of iPSCs, we found that telomerase plays a critical role in reprogramming and self-renewal of iPSCs. Further, telomerase maintenance of telomeres is necessary for induction of true pluripotency while the alternative pathway of elongation and maintenance by recombination is also required, but not sufficient. Together, several aspects of telomere biology may account for the variable telomere dynamics in iPSCs. Notably, the mechanisms employed to maintain telomeres during iPSC reprogramming are very similar to those of embryonic stem cells. These findings may also relate to the cloning field where these mechanisms could be responsible for telomere heterogeneity after nuclear reprogramming by somatic cell nuclear transfer.

Indexed as

AnimalsCell DifferentiationCells, CulturedCellular ReprogrammingEmbryonic Stem CellsFibroblastsGene ExpressionInduced Pluripotent Stem CellsIn Situ Hybridization, FluorescenceMiceRecombination, GeneticTelomeraseTelomereTelomere HomeostasisTranscription FactorsTelomeraseTranscription FactorsZscan4d protein, mouse

Identifiers

PMID22184006
PMCPMC3317559

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.