Phosphorylation Promotes the Accumulation of PERIOD Protein Foci  

在线阅读下载全文

作  者:Mengna Li Shujing Li Luoying Zhang 

机构地区:[1]Key Laboratory of Molecular Biophysics of Ministry of Education,College of Life Science and TechnologyHuazhong University of Science and Technology,Wuhan,Hubei 430074,China [2]Department of Life Sciences,Bengbu Medical College,Bengbu,Anhui 233030,China [3]Hubei Province Key Laboratory of Oral and Maxillofacial Development and Regeneration,Wuhan,Hubei 430022,China

出  处:《Research》2024年第1期59-69,共11页研究(英文)

基  金:grants from the Natural Science Foundation of China(3193002i and 32022035);the Ministry of Science and Technology of China STI 2030-Major Projects(2021ZD0203200-02)to L.Z.

摘  要:Circadian clock drives the 24-h rhythm in our behavior and physiology.The molecular clock consists of a series of transcriptional/translational feedback loops operated by a number of clock genes.A very recent study reported that the clock protein PERIOD(PER)is organized into discrete foci at the nuclear envelope in fly circadian neurons,which is believed to be important for controlling the subcellular localization of clock genes.Loss of inner nuclear membrane protein lamin B receptor(LBR)leads to disruption of these foci,but how they are regulated is yet unknown.Here,we found that PER foci are likely phase-separated condensates,the formation of which is mediated by intrinsically disordered region in PER.Phosphorylation promotes the accumulation of these foci.Protein phosphatase 2A,which is known to dephosphorylate PER,hampers the accumulation of the foci.On the other hand,the circadian kinase DOUBLETIME(DBT)which phosphorylates PER enhances the accumulation of the foci.LBR likely facilitates PER foci accumulation by destabilizing the catalytic subunit of protein phosphatase 2A,MICROTUBULE STAR(MTS).In conclusion,here,we demonstrate a key role for phosphorylation in promoting the accumulation of PER foci,while LBR modulates this process by impinging on the circadian phosphatase MTS.

关 键 词:CONCLUSION SEPARATED TRANSLATIONAL 

分 类 号:O57[理学—粒子物理与原子核物理]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象