Literature DB >> 22735032

Reference genes in the developing murine brain and in differentiating embryonic stem cells.

Nadine Kraemer1, Gerda Neubert, Lina Issa, Olaf Ninnemann, Andrea E M Seiler, Angela M Kaindl.   

Abstract

OBJECTIVES: Gene expression analysis via quantitative real-time PCR (qPCR) is a key approach in biological and medical research. Here, variations between runs and samples are compensated for by in-parallel analysis of reference genes, which require a most stable expression throughout all samples and experimental procedures to function as internal standards. In reality, there is no universal reference gene; but rather, assumed reference genes vary widely among various cell types. This demands an evaluation of reference genes for each specific experimental purpose, especially in the case of developmental studies. The aim of the present study was to identify suitable reference genes for gene expression analysis in the developing murine brain neocortex in vivo and in mouse embryonic stem cells (mESC) throughout differentiation in vitro.
METHODS: The five candidate genes Actb, 18s, Gapdh, Hprt, and RpII were analyzed throughout development in vivo and in vitro using the quartiles of C(q) values, fold change, coefficient of variation (CV) and the difference between maximum minus twofold standard deviation and mean as the criteria to evaluate their expression stability.
RESULTS: We found that RpII was the most stable expressed gene in mESC throughout differentiation, while in the developing murine neocortex Gapdh showed the highest expression stability.
CONCLUSIONS: Based on our results, we suggest for gene expression analysis in the context of neurodevelopment the usage of RpII as a reference gene for mESC and Gapdh or Hprt for the murine neocortex.

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Year:  2012        PMID: 22735032     DOI: 10.1179/1743132812Y.0000000060

Source DB:  PubMed          Journal:  Neurol Res        ISSN: 0161-6412            Impact factor:   2.448


  8 in total

1.  Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytes.

Authors:  Nadine Kraemer; Ethiraj Ravindran; Sami Zaqout; Gerda Neubert; Detlev Schindler; Olaf Ninnemann; Ralph Gräf; Andrea E M Seiler; Angela M Kaindl
Journal:  Cell Cycle       Date:  2015       Impact factor: 4.534

2.  The Rat Homolog of the Schizophrenia Susceptibility Gene ZNF804A Is Highly Expressed during Brain Development, Particularly in Growth Cones.

Authors:  Katja Hvid Hinna; Karen Rich; Åsa Fex-Svenningsen; Eirikur Benedikz
Journal:  PLoS One       Date:  2015-07-06       Impact factor: 3.240

3.  Mutations in PTRH2 cause novel infantile-onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weakness.

Authors:  Hao Hu; Michelle L Matter; Lina Issa-Jahns; Mayumi Jijiwa; Nadine Kraemer; Luciana Musante; Michelle de la Vega; Olaf Ninnemann; Detlev Schindler; Natalia Damatova; Katharina Eirich; Marco Sifringer; Sandra Schrötter; Britta J Eickholt; Lambert van den Heuvel; Chanel Casamina; Gisela Stoltenburg-Didinger; Hans-Hilger Ropers; Thomas F Wienker; Christoph Hübner; Angela M Kaindl
Journal:  Ann Clin Transl Neurol       Date:  2014-12-03       Impact factor: 4.511

4.  Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation.

Authors:  Ethiraj Ravindran; Hao Hu; Scott A Yuzwa; Luis R Hernandez-Miranda; Nadine Kraemer; Olaf Ninnemann; Luciana Musante; Eugen Boltshauser; Detlev Schindler; Angela Hübner; Hans-Christian Reinecker; Hans-Hilger Ropers; Carmen Birchmeier; Freda D Miller; Thomas F Wienker; Christoph Hübner; Angela M Kaindl
Journal:  PLoS Genet       Date:  2017-04-28       Impact factor: 5.917

5.  Differential Effects of Resveratrol on the Expression of Brain-Derived Neurotrophic Factor Transcripts and Protein in the Hippocampus of Rat Brain.

Authors:  Shahla Shojaei; Mohammad Reza Panjehshahin; Sayed Mohammad Shafiee; Zahra Khoshdel; Mohammad Borji; Ghasem Ghasempour; Ali Akbar Owji
Journal:  Iran J Med Sci       Date:  2017-01

6.  Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability.

Authors:  Ethiraj Ravindran; Cynthia Gutierrez de Velazco; Ali Ghazanfar; Nadine Kraemer; Sami Zaqout; Abdul Waheed; Mohsan Hanif; Sadia Mughal; Alessandro Prigione; Na Li; Xiang Fang; Hao Hu; Angela M Kaindl
Journal:  J Med Genet       Date:  2021-05-31       Impact factor: 5.941

7.  Chemokine (C-C Motif) Receptor-Like 2 is not essential for lung injury, lung inflammation, or airway hyperresponsiveness induced by acute exposure to ozone.

Authors:  Farhan Malik; Kevin R Cromar; Constance L Atkins; Roger E Price; William T Jackson; Saad R Siddiqui; Chantal Y Spencer; Nicholas C Mitchell; Ikram U Haque; Richard A Johnston
Journal:  Physiol Rep       Date:  2017-12

8.  Selection of Reliable Reference Genes for Analysis of Gene Expression in Spinal Cord during Rat Postnatal Development and after Injury.

Authors:  Ján Košuth; Martina Farkašovská; Filip Mochnacký; Zuzana Daxnerová; Juraj Ševc
Journal:  Brain Sci       Date:  2019-12-20
  8 in total

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