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Investigation of microRNA expression and DNA repair gene transcripts in human oocytes and blastocysts.
Tulay, P; Naja, R P; Cascales-Roman, O; Doshi, A; Serhal, P; SenGupta, S B.
Affiliation
  • Tulay P; Faculty of Medicine, Medical Genetics Department, Near East University, Yakin Dogu Bulvari, Nicosia, Cyprus. pintulay@gmail.com.
  • Naja RP; UCL Centre for PGD, Institute for Women's Health, University College London, London, UK. pintulay@gmail.com.
  • Cascales-Roman O; UCL Centre for PGD, Institute for Women's Health, University College London, London, UK.
  • Doshi A; UCL Centre for PGD, Institute for Women's Health, University College London, London, UK.
  • Serhal P; The Centre for Reproductive and Genetic Health, University College Hospital, The New Wing Eastman Dental Hospital, London, UK.
  • SenGupta SB; The Centre for Reproductive and Genetic Health, University College Hospital, The New Wing Eastman Dental Hospital, London, UK.
J Assist Reprod Genet ; 32(12): 1757-64, 2015 Dec.
Article in En | MEDLINE | ID: mdl-26438643
ABSTRACT

PURPOSE:

The aim of the study is to investigate the regulation of DNA repair genes by microRNAs (miRNAs). miRNAs are short non-coding RNAs that regulate transcriptional and post-transcriptional gene silencing. Several miRNAs that are expressed during preimplantation embryo development have been shown or are predicted to target genes that regulate cell cycle checkpoints and DNA repair in response to DNA damage.

METHODS:

This study compares the expression level of 20 miRNAs and 9 target transcripts involved in DNA repair. The statistical significance of differential miRNA expression between oocytes and blastocysts was determined by t test analysis using the GraphPad Prism v6 software. The possible regulatory roles of miRNAs on their target messenger RNAs (mRNAs) were analysed using a Pearson correlation test.

RESULTS:

This study shows for the first time that several miRNAs are expressed in human oocytes and blastocysts that target key genes involved in DNA repair and cell cycle checkpoints. Blastocysts exhibited statistically significant lower expression levels for the majority of miRNAs compared to oocytes (p < 0.05). Correlation analyses showed that there was both inverse and direct association between miRNAs and their target mRNAs.

CONCLUSIONS:

miRNAs target many mRNAs including ones involved in DNA repair mechanisms. This study suggests that miRNAs and their target mRNAs involved in DNA repair are expressed in preimplantation embryos. Similar to the miRNAs expressed in adult tissues, these miRNAs seem to have regulatory roles on their target DNA repair mRNAs during preimplantation embryo development.
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Full text: 1 Database: MEDLINE Main subject: Oocytes / Blastocyst / MicroRNAs / DNA Repair Limits: Adult / Humans Language: En Journal: J Assist Reprod Genet Journal subject: GENETICA / MEDICINA REPRODUTIVA Year: 2015 Type: Article Affiliation country: Cyprus

Full text: 1 Database: MEDLINE Main subject: Oocytes / Blastocyst / MicroRNAs / DNA Repair Limits: Adult / Humans Language: En Journal: J Assist Reprod Genet Journal subject: GENETICA / MEDICINA REPRODUTIVA Year: 2015 Type: Article Affiliation country: Cyprus