Role of TRF2 and TPP1 regulation in idiopathic recurrent pregnancy loss.


Journal

International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578

Informations de publication

Date de publication:
15 Apr 2019
Historique:
received: 27 07 2018
revised: 31 12 2018
accepted: 03 01 2019
pubmed: 7 1 2019
medline: 20 6 2019
entrez: 7 1 2019
Statut: ppublish

Résumé

Telomeres are the tandem repeats (TTAGGG) present at the ends of the chromosomes that ensure chromosome stability and protect chromosomes from degradation. Telomeres in somatic human cells shorten after every cellular division and are linked to the cellular senescence. In this study we have investigated telomere length and expression of shelterin genes in aborted fetus material from idiopathic recurrent pregnancy losses. Telomere length was measured using Telomere Restriction Fragment Length (TRF) analysis. The gene expression levels for important shelterin complex proteins (TRF1, TRF2, POT1, and TPP1) were determined by Real-time Quantitative Reverse Transcriptase PCR (qRT-PCR). Our results demonstrated down regulation of TRF2 and TPP1 and a strong decline in average telomere length in abort material from women suffering from idiopathic recurrent pregnancy loss. We suggest that shorter telomere length and downregulation of the major shelterin components TRF2 and TPP1 leading to "telomere uncapping", might play a critical role in recurrent pregnancy loss.

Identifiants

pubmed: 30611803
pii: S0141-8130(18)33879-0
doi: 10.1016/j.ijbiomac.2019.01.011
pii:
doi:

Substances chimiques

ACD protein, human 0
Shelterin Complex 0
TERF2 protein, human 0
Telomere-Binding Proteins 0
Telomeric Repeat Binding Protein 2 0
Aminopeptidases EC 3.4.11.-
Dipeptidyl-Peptidases and Tripeptidyl-Peptidases EC 3.4.14.-

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

306-310

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

Auteurs

Rameez Hassan Pirzada (RH)

Near East University, Faculty of Medicine, Department of Medical Genetics, 999058 Nicosia, North Cyprus, Turkey; Institute of Molecular Biology and Biotechnology, The University of Lahore, New Campus, Lahore 55150, Pakistan.

Oya Orun (O)

Marmara University School of Medicine, Biophysics Department, Istanbul, Turkey.

Can Erzik (C)

Marmara University School of Medicine, Department of Medical Biology, Istanbul, Turkey.

Huseyin Cagsin (H)

Near East University, Faculty of Medicine, Department of Medical Genetics, 999058 Nicosia, North Cyprus, Turkey; Near East University, Faculty of Art and Sciences, Department of Molecular Biology and Genetics, 999058 Nicosia, North Cyprus, Turkey.

Nedime Serakinci (N)

Near East University, Faculty of Medicine, Department of Medical Genetics, 999058 Nicosia, North Cyprus, Turkey; Near East University, Faculty of Art and Sciences, Department of Molecular Biology and Genetics, 999058 Nicosia, North Cyprus, Turkey. Electronic address: nedime.serakinci@neu.edu.tr.

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Classifications MeSH