TY - JOUR
T1 - Differences in embryo quality are associated with differences in oocyte composition
T2 - a proteomic study in inbred mice
AU - Pfeiffer, Martin J
AU - Taher, Leila
AU - Drexler, Hannes
AU - Suzuki, Yutaka
AU - Makałowski, Wojciech
AU - Schwarzer, Caroline
AU - Wang, Bingyuan
AU - Fuellen, Georg
AU - Boiani, Michele
N1 - © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2015/2
Y1 - 2015/2
N2 - Current models of early mouse development assign roles to stochastic processes and epigenetic regulation, which are considered to be as influential as the genetic differences that exist between strains of the species Mus musculus. The aim of this study was to test whether mouse oocytes vary from each other in the abundance of gene products that could influence, prime, or even predetermine developmental trajectories and features of derivative embryos. Using the paradigm of inbred mouse strains, we quantified 2010 protein groups (SILAC LC-MS/MS) and 15205 transcripts (RNA deep sequencing) present simultaneously in oocytes of four strains tested (129/Sv, C57Bl/6J, C3H/HeN, DBA/2J). Oocytes differed according to donor strain in the abundance of catalytic and regulatory proteins, as confirmed for a subset (bromodomain adjacent to zinc finger domain, 1B [BAZ1B], heme oxygenase 1 [HMOX1], estrogen related receptor, beta [ESRRB]) via immunofluorescence in situ. Given a Pearson's r correlation coefficient of 0.18-0.20, the abundance of oocytic proteins could not be predicted from that of cognate mRNAs. Our results document that a prerequisite to generate embryo diversity, namely the different abundances of maternal proteins in oocytes, can be studied in the model of inbred mouse strains. Thus, we highlight the importance of proteomic quantifications in modern embryology. All MS data have been deposited in the ProteomeXchange with identifier PXD001059 (http://proteomecentral.proteomexchange.org/dataset/PXD001059).
AB - Current models of early mouse development assign roles to stochastic processes and epigenetic regulation, which are considered to be as influential as the genetic differences that exist between strains of the species Mus musculus. The aim of this study was to test whether mouse oocytes vary from each other in the abundance of gene products that could influence, prime, or even predetermine developmental trajectories and features of derivative embryos. Using the paradigm of inbred mouse strains, we quantified 2010 protein groups (SILAC LC-MS/MS) and 15205 transcripts (RNA deep sequencing) present simultaneously in oocytes of four strains tested (129/Sv, C57Bl/6J, C3H/HeN, DBA/2J). Oocytes differed according to donor strain in the abundance of catalytic and regulatory proteins, as confirmed for a subset (bromodomain adjacent to zinc finger domain, 1B [BAZ1B], heme oxygenase 1 [HMOX1], estrogen related receptor, beta [ESRRB]) via immunofluorescence in situ. Given a Pearson's r correlation coefficient of 0.18-0.20, the abundance of oocytic proteins could not be predicted from that of cognate mRNAs. Our results document that a prerequisite to generate embryo diversity, namely the different abundances of maternal proteins in oocytes, can be studied in the model of inbred mouse strains. Thus, we highlight the importance of proteomic quantifications in modern embryology. All MS data have been deposited in the ProteomeXchange with identifier PXD001059 (http://proteomecentral.proteomexchange.org/dataset/PXD001059).
KW - Animals
KW - Embryo, Mammalian/chemistry
KW - Embryonic Development/physiology
KW - Female
KW - Gene Expression Profiling
KW - Gene Expression Regulation, Developmental
KW - High-Throughput Nucleotide Sequencing
KW - Isotope Labeling
KW - Male
KW - Mass Spectrometry
KW - Mice
KW - Mice, Inbred Strains/embryology
KW - Oocytes/chemistry
KW - Proteome/analysis
KW - Proteomics
KW - Reproducibility of Results
KW - Sequence Analysis, RNA
KW - Transcriptome
U2 - 10.1002/pmic.201400334
DO - 10.1002/pmic.201400334
M3 - Article
C2 - 25367296
VL - 15
SP - 675
EP - 687
JO - Proteomics
JF - Proteomics
SN - 1615-9853
IS - 4
ER -