Zebrafish is an important vertebrate model system for understanding early embryogenesis. Genome analysis shows that 71% of human genes have at least one ortholog in zebrafish and 82% of the known genes responsible for human disease are present in zebrafish. Research on zebrafish embryos could shed invaluable light on human early embryogenesis. There is a rich literature on transcriptome-wide changes that accompany zebrafish early embryogenesis. However, transcriptome-level information is limited because zygotic transcription is silent before the mid-blastula transition (MBT), because post-transcriptional regulation modulates gene expression, and because protein post-translational modifications (PTMs) influence protein function. We hypothesize that high time- and spatial-resolution studies of the early-stage zebrafish proteome will provide new insights into early embryogenesis.

Public Health Relevance

We will reveal the proteome dynamics of zebrafish early-stage embryos with high time and spatial resolution. The results are invaluable for accurate understanding of the important events during early embryogenesis, e.g., early cellular differentiation and early organogenesis. The studies will generate a list of important gene targets for further gene mutation studies for understanding how gene mutations lead to birth defects.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM125991-03S1
Application #
10145967
Study Section
Program Officer
Krepkiy, Dmitriy
Project Start
2018-01-01
Project End
2022-12-31
Budget Start
2020-01-01
Budget End
2020-12-31
Support Year
3
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Michigan State University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
Shen, Xiaojing; Sun, Liangliang (2018) Systematic Evaluation of Immobilized Trypsin-Based Fast Protein Digestion for Deep and High-Throughput Bottom-Up Proteomics. Proteomics 18:e1700432
Chen, Daoyang; Shen, Xiaojing; Sun, Liangliang (2018) Strong cation exchange-reversed phase liquid chromatography-capillary zone electrophoresis-tandem mass spectrometry platform with high peak capacity for deep bottom-up proteomics. Anal Chim Acta 1012:1-9
Li, Ziwei; He, Bo; Kou, Qiang et al. (2018) Evaluation of top-down mass spectral identification with homologous protein sequences. BMC Bioinformatics 19:494
McCool, Elijah N; Lubeckyj, Rachele A; Shen, Xiaojing et al. (2018) Deep Top-Down Proteomics Using Capillary Zone Electrophoresis-Tandem Mass Spectrometry: Identification of 5700 Proteoforms from the Escherichia coli Proteome. Anal Chem 90:5529-5533
McCool, Elijah N; Lubeckyj, Rachele; Shen, Xiaojing et al. (2018) Large-scale Top-down Proteomics Using Capillary Zone Electrophoresis Tandem Mass Spectrometry. J Vis Exp :
Shen, Xiaojing; Kou, Qiang; Guo, Ruiqiong et al. (2018) Native Proteomics in Discovery Mode Using Size-Exclusion Chromatography-Capillary Zone Electrophoresis-Tandem Mass Spectrometry. Anal Chem 90:10095-10099
Yang, Zhichang; Shen, Xiaojing; Chen, Daoyang et al. (2018) Microscale Reversed-Phase Liquid Chromatography/Capillary Zone Electrophoresis-Tandem Mass Spectrometry for Deep and Highly Sensitive Bottom-Up Proteomics: Identification of 7500 Proteins with Five Micrograms of an MCF7 Proteome Digest. Anal Chem 90:10479-10486