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Updated: May 22, 2025

Primary Endodermal Epithelial Cell Culture from the Yolk Sac Membrane of Japanese Quail Embryos
Published on: March 10, 2016
Study on yolk iron transportation in chick embryo eggs based on transcriptomics
Lulu Ma1, Zhaowei Cui2, Shuaishuai Wei1
1Engineering Research Center of Bio-process, Ministry of Education/ School of Food and Biological Engineering, Hefei University of Technology, Hefei 230601, China; Key Laboratory for Agricultural Products Processing of Anhui Province/Key Laboratory for Animal Food Green Manufacturing and Resource Mining of Anhui Province, Hefei 230601, China.
Insights
Chick embryos utilize a complete iron system for rapid absorption. From day 9 to 12, divalent metal transporter 1 (DMT1) and ferritin heavy chain 1 (FTH1) are crucial for initiating iron transport during incubation.
Area of Science:
- Developmental Biology
- Nutritional Science
- Molecular Biology
Background:
- Chick embryos possess a comprehensive system for iron metabolism, making them an ideal model for studying iron transport and absorption.
- Understanding iron regulation during embryonic development is critical for avian health and nutrition.
Purpose of the Study:
- To investigate the regulatory genes and pathways involved in iron transportation and uptake during key stages of chick embryo development (E6, E9, E12, E15).
- To identify critical periods and molecular players in embryonic iron acquisition.
Main Methods:
- Transcriptome analysis was performed on chick embryos at days 6, 9, 12, and 15 of incubation.
- Iron content was measured in egg yolk, embryo, and yolk sac membrane (YSM).
- Gene expression levels of key iron-related transporters and storage proteins were analyzed.
Main Results:
- Iron content decreased in the yolk while increasing in the embryo, with a transient peak in the YSM at E12.
- Transcriptome analysis revealed 87,499 expressed genes, with stage-specific gene expression patterns.
- Mineral absorption pathways were significantly enriched from E9 to E15.
- Expression of divalent metal transporter 1 (DMT1) and ferritin heavy chain 1 (FTH1) increased significantly from E9 to E12.
- Genes such as Heme oxygenase 1 (HMOX1), FTH1, Solute Carrier Family 40 Member 1 (SLC40A1), and hephaestin (HEPH) were upregulated from E12 to E15.
Conclusions:
- The period between embryonic days 9 and 12 represents a crucial phase for iron initiation and transport.
- DMT1 and FTH1 are key regulators of iron transport initiation in early chick embryonic development.
- The study elucidates the dynamic changes and molecular mechanisms governing iron homeostasis during chick embryogenesis.
Abstract:
Chick embryo eggs have a complete system of iron release, delivery, and uptake and thus provide a useful tool to study the fast transportation and absorption of iron. Based on this, the regulatory genes and pathways of iron transportation and uptake at the four key stages of chick embryo incubation, days 6, 9, 12, and 15 (E6, E9, E12, and E15), were investigated. Throughout these four key stages, the iron content decreased in egg yolk, increased in chick embryos, and first increased and then decreased in the yolk sac membrane (YSM) with the highest value of 110.38 mg/kg at E12. A total of 87,499 expressed genes were detected by transcriptome, where the specifically expressed genes at E6, E9, E12, and E15 were 312, 466, 280, and 185 respectively. Mineral absorption pathways involved in mineral uptake, transportation, utilization, and metabolism were significantly enriched in stages E9 to E15. The expression of divalent metal transporter 1 (DMT1) and ferritin heavy chain 1 (FTH1) related to iron transportation was up-regulated considerably from E9 to E12. Heme oxygenase 1 (HMOX1), FTH1, Solute Carrier Family 40 Member 1 (SLC40A1), and hephaestin (HEPH) mainly responsible for the regulation of iron transportation and uptake were up-regulated from E12 to E15. Therefore, stage E9 to E12 was the crucial period for iron initiation and transportation, and DMT1 and FTH1 played an important role in regulating the initiation of iron transportation at the early stage of incubation.

