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Updated: Feb 19, 2026

Analysis of Cell Differentiation, Morphogenesis, and Patterning During Chicken Embryogenesis Using the Soaked-Bead Assay
Published on: January 12, 2022
CCDC134 serves a crucial role in embryonic development
Biaoyi Yu1, Tianzhuo Zhang1, Peng Xia1
1Department of Immunology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100191, P.R. China.
Coiled-coil domain containing 134 (CCDC134) is crucial for embryonic development, with its absence causing severe developmental defects and embryonic lethality in mice. This highlights CCDC134's essential role in early development.
Area of Science:
- Developmental Biology
- Immunology
- Molecular Biology
Background:
- Coiled-coil domain containing 134 (CCDC134) is a secreted protein with potential roles in immune responses and antitumor activity.
- CCDC134 may also regulate human activation/deficiency 2a and influence the p300-CBP-associated factor complex's acetyltransferase activity.
Purpose of the Study:
- To investigate the biological and pathological functions of CCDC134 during embryonic development.
- To generate a conditional knockout mouse model for temporal and spatial control of Ccdc134 gene ablation.
Main Methods:
- Generation of a Ccdc134fl/fl conditional knockout mouse strain.
- Crossing Ccdc134fl/fl mice with Cre-driver lines (human β-actin-Cre or zona pellucida 3-Cre) to achieve gene ablation.
- Analysis of embryonic lethality, developmental abnormalities, and cellular defects in Ccdc134-/- embryos.
Main Results:
- Ccdc134-/- embryos exhibited embryonic lethality between E12.5 and birth.
- Absence of CCDC134 led to severe hemorrhages, abnormal organ development (liver, heart), and placental issues.
- Reduced cell proliferation and vascular endothelial cell defects were observed in E13.5 fetal tissues.
- CCDC134 demonstrated dynamic and specific expression patterns during embryonic development.
Conclusions:
- CCDC134 plays a critical and essential role in mouse embryonic development.
- Loss of CCDC134 results in severe developmental defects, leading to embryonic lethality.
- Further research is warranted to elucidate the precise mechanisms by which CCDC134 regulates embryonic development.
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