Long noncoding RNA DREAMer bridges the DREAM complex and E2f1 to regulate endoreplication in Drosophila

被引:0
|
作者
Li, Dong [1 ]
Jin, Tianyu [2 ]
Liu, Jun [1 ]
Lu, Chunlin [2 ]
Yang, Xianmei [2 ]
Zhang, Haiyan [1 ]
Bi, Limin [1 ]
Yan, Yuhang [1 ]
Zhang, Lijiao [1 ]
Sang, Yan [3 ]
Jin, Bilian [4 ]
Bi, Xiaolin [1 ]
机构
[1] Nantong Univ, Sch Med, Nantong 226001, Peoples R China
[2] Dalian Med Univ, Coll Basic Med Sci, Dalian 116044, Peoples R China
[3] Nantong Univ, Affiliated Hosp, Comp Technol Ctr, Sch Med, Nantong 226001, Peoples R China
[4] Dalian Med Univ, Inst Canc Stem Cell, Dalian 116044, Peoples R China
来源
SCIENCE ADVANCES | 2024年 / 10卷 / 45期
基金
中国国家自然科学基金;
关键词
TRANSCRIPTION FACTOR; PROTEINS; MYB; IDENTIFICATION; ANTAGONISM; POLYPLOIDY; EXPRESSION; INSIGHTS; FAMILY; GENES;
D O I
10.1126/sciadv.adr4936
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Rb/E2f and DREAM complexes play vital roles in regulating cell cycle progression. To date, how they coordinate their functions to regulate cell cycle-dependent gene expression is not clear. Here, we identified a long noncoding RNA (lncRNA), which we named DREAMer, that bridges the interaction between E2f1 and the dREAM complex to regulate endoreplication specifically in Drosophila salivary gland. We show that E2f1 directly stimulates DREAMer expression, whereas DREAMer mediates the repression of e2f1 transcription by modulating the recruitment of the dREAM complex to the e2f1 promoter via a direct interaction with the dREAM component E2f2. The depletion of DREAMer impairs dREAM binding, leading to derepression of e2f1 transcription, which ultimately increases E2f1 activity and promotes the endoreplication. Furthermore, the transcriptomic analysis revealed profound changes in cell cycle-related gene expression in DREAMerKO salivary glands. Together, our findings reveal an lncRNA-mediated link between the dREAM complex and E2f1, which regulates endoreplication during development.
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页数:15
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