Acquisition of pluripotency in the chick embryo occurs during intrauterine embryonic development via a unique transcriptional network

被引:10
作者
Han, Jae Yong [1 ,2 ,3 ]
Lee, Hyo Gun [1 ,2 ]
Park, Young Hyun [1 ,2 ]
Hwang, Young Sun [1 ,2 ]
Kim, Sang Kyung [1 ,2 ]
Rengaraj, Deivendran [4 ]
Cho, Byung Wook [5 ]
Lim, Jeong Mook [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Agr & Life Sci, Dept Agr Biotechnol, Seoul 08826, South Korea
[2] Seoul Natl Univ, Coll Agr & Life Sci, Res Inst Agr & Life Sci, Seoul 08826, South Korea
[3] Shinshu Univ, Inst Biomed Sci, Minamiminowa, Nagano 3994598, Japan
[4] Chung Ang Univ, Dept Anim Sci & Technol, Anseong 17546, Gyeonggi Do, South Korea
[5] Pusan Natl Univ, Coll Nat Resources & Life Sci, Dept Anim Sci, Miryang 50463, South Korea
来源
JOURNAL OF ANIMAL SCIENCE AND BIOTECHNOLOGY | 2018年 / 9卷
基金
新加坡国家研究基金会;
关键词
Avian; Embryonic development; NANOG; Pluripotency; Transcriptional factor; COMPLEMENTARY NORMAL TABLE; PRIMITIVE STREAK FORMATION; TO-ZYGOTIC TRANSITION; PRIMORDIAL GERM-CELLS; STEM-CELLS; PROTEIN-SYNTHESIS; GENE-EXPRESSION; SOX3; GENES; 1ST STAGES; ES CELLS;
D O I
10.1186/s40104-018-0246-0
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Background: Acquisition of pluripotency by transcriptional regulatory factors is an initial developmental event that is required for regulation of cell fate and lineage specification during early embryonic development. The evolutionarily conserved core transcriptional factors regulating the pluripotency network in fishes, amphibians, and mammals have been elucidated. There are also species-specific maternally inherited transcriptional factors and their intricate transcriptional networks important in the acquisition of pluripotency. In avian species, however, the core transcriptional network that governs the acquisition of pluripotency during early embryonic development is not well understood. Results: We found that chicken NANOG (cNANOG) was expressed in the stages between the pre-ovulatory follicle and oocyte and was continuously detected in Eyal-Giladi and Kochav stage I (EGK.I) to X. However, cPOUV was not expressed during folliculogenesis, but began to be detectable between EGK.V and VI. Unexpectedly, cSOX2 could not be detected during folliculogenesis and intrauterine embryonic development. Instead of cSOX2, cSOX3 was maternally inherited and continuously expressed during chicken intrauterine development. In addition, we found that the pluripotency-related genes such as cENS-1, cKIT, cLIN28A, cMYC, cPRDM14, and cSALL4 began to be dramatically upregulated between EGK.VI and VIII. Conclusion: These results suggest that chickens have a unique pluripotent circuitry since maternally inherited cNANOG and cSOX3 may play an important role in the initial acquisition of pluripotency. Moreover, the acquisition of pluripotency in chicken embryos occurs at around EGK.VI to VIII.
引用
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页数:11
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