<scp>PELO</scp> regulates erythroid differentiation through interaction with <scp>MYC</scp> to upregulate <scp>KLF10</scp>

Erythropoiesis is a multistep process of erythroid cell production that is controlled by multiple regulatory factors. Ribosome rescue factor PELO plays a crucial role in cell meiotic division and mice embryonic development. However, the function of PELO in erythroid differentiation remains unclear. Here, we showed that knockdown of PELO increased hemin-induced erythroid differentiation of K562 and HEL cells, exhibiting a higher number of benzidine-positive cells and increased mRNA levels of erythroid genes. PELO knockdown inhibited the proliferation and cell cycle progression and promoted apoptosis of K562 cells. Mechanistically, PELO could regulate the expression of KLF10 through interaction with MYC. Moreover, KLF10 knockdown also enhanced erythroid differentiation of K562 and HEL cells induced by hemin. Collectively, our results demonstrated that PELO regulates erythroid differentiation and increases KLF10 expression levels by interacting with MYC.

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Publication Details

Journal
FEBS Journal
Published
2024-08-29
DOI
https://doi.org/10.1111/febs.17254
Primary Topic
Kruppel-like factors research
Type
article
Field-Weighted Citation Impact
0.00

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article

PELO regulates erythroid differentiation through interaction with MYC to upregulate KLF10

Jinglan Hao, Naer Sa, Ping Gao, Xiaoming Dong et al.
FEBS Journal
Kruppel-like factors research
article

PELO regulates erythroid differentiation through interaction with MYC to upregulate KLF10

Jinglan Hao, Naer Sa, Ping Gao, Xiaoming Dong, Chen Huang, Kai Zhang, Zhongqi Li, Guiqin Han, Hang Hu, Xin Liang, Yongtong Ruan, Bixi Hu
article en

Abstract

Erythropoiesis is a multistep process of erythroid cell production that is controlled by multiple regulatory factors. Ribosome rescue factor PELO plays a crucial role in cell meiotic division and mice embryonic development. However, the function of PELO in erythroid differentiation remains unclear. Here, we showed that knockdown of PELO increased hemin-induced erythroid differentiation of K562 and HEL cells, exhibiting a higher number of benzidine-positive cells and increased mRNA levels of erythroid genes. PELO knockdown inhibited the proliferation and cell cycle progression and promoted apoptosis of K562 cells. Mechanistically, PELO could regulate the expression of KLF10 through interaction with MYC. Moreover, KLF10 knockdown also enhanced erythroid differentiation of K562 and HEL cells induced by hemin. Collectively, our results demonstrated that PELO regulates erythroid differentiation and increases KLF10 expression levels by interacting with MYC.

FEBS JournalVol. 291(21)
Hansoh Bio (United States), Shaanxi Normal University (CN)
Shaanxi Normal University, Natural Science Foundation of Shaanxi Province, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 87%
Kruppel-like factors research
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