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Zebrafish mutants in egln1 display a hypoxic response and develop polycythemia

Life Sci. 2024-03; 
Xuehan Dou, Zhongyuan Chen, Yunzhang Liu, Yun Li, Junli Ye, Ling Lu
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Mutant Libraries … The Cas9 protein was from GenScript (#Z03389, Nanjing, China). Mutant screening was performed following the methods described in a previous study [17]. The genotyping PCR … Get A Quote

摘要

objective: Prolyl hydroxylase domain 2 (PHD2), encoded by the Egln1 gene, serves as a pivotal regulator of the hypoxia-inducible factor (HIF) pathway and acts as a cellular oxygen sensor. Somatic inactivation of Phd2 in mice results in polycythemia and congestive heart failure. However, due to the embryonic lethality of Phd2 deficiency, its role in development remains elusive. Here, we investigated the function of two egln1 paralogous genes, egln1a and egln1b, in zebrafish. methods: The egln1 null zebrafish were generated using the CRISPR/Cas9 system. Quantitative real-time PCR assays and Western blot analysis were employed to detect the effect of egln1 deficiency on the hypoxia signaling pathway. The hypoxia r... More

關鍵詞

Hypoxia, Polycythemia, Zebrafish, egln1a, egln1b, hif
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