Effects of P27/Bmdacapo, in the CIP/KIP family, on cell proliferation, growth and development in the silkworm (Bombyx mori)

被引:1
作者
Li, Niannian [1 ]
Meng, Gang [1 ]
Tong, Xiaoling [1 ]
Sun, Fuze [1 ]
Zeng, Jie [1 ]
Bai, Yanmin [1 ]
Liang, Shubo [1 ]
Hu, Hai [1 ]
Liu, Lanlan [1 ]
Han, Minjin [1 ]
Lu, Cheng [1 ]
Dai, Fangyin [1 ]
机构
[1] Southwest Univ, Minist Agr, Key Lab Sericultural Biol & Genet Breeding, Coll Biotechnol,State Key Lab Silkworm Genome Bio, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
P27/Dacapo; Silkworm; CIP/KIP family; Gu/S; Cell cycle; Development; DEPENDENT KINASE INHIBITOR; IN-VIVO; CYCLIN; P27; EXPRESSION; P27(KIP1); APOPTOSIS; ARREST; DACAPO; LUNG;
D O I
10.1016/j.gene.2019.02.087
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We investigated changes in expression of the CIP/KIP family-related genes and the cycle-dependent factors Pena, Cdk4 and Cdk2 during the growth and development of mice, Drosophila and silkworms. When the organism was in a period of rapid development, the related genes of the CIP/KIP family had low expression level and the cell cycle-dependent genes were highly expressed. In mammals, the CIP/KIP family includes three genes, p21, p27/Dacapo and p57. However, only one gene, P27/Dacapo, exists in the CIP/KIP family in silkworm' and the orthologous gene in the silkworm is named Bmdacapo. Down-regulation of Bmdacapo in silkworm embryos caused overdevelopment of the embryos and indicated that Bmdacapo can inhibit silkworm growth and development. Up-regulation of Bmdacapo in silkworm cells inhibited cell proliferation, whereas down-regulation of Bmdacapo promoted cell proliferation. In order to explore the mechanism of Bmdacapo regulated silkworm development and cell proliferation, the effect of Bmdacapo on cell cycle changes was examined. The results demonstrate that Bmdacapo was able to induce G1/S phase arrest in the cell cycle. In silkworm cells, Bmdacapo inhibits the expression of Pcna, CDK4 and CDK2, which affects the cell cycle and ultimately inhibits cell proliferation. This regulatory mechanism is particularly different from mammals.
引用
收藏
页码:31 / 37
页数:7
相关论文
共 32 条
[1]   Direct interactions with both p27 and Cdk2 regulate Spy1-mediated proliferation in vivo and in vitro [J].
Al Sorkhy, Mohammad ;
Fifield, Bre-Anne ;
Myers, Dorothy ;
Porter, Lisa A. .
CELL CYCLE, 2016, 15 (01) :128-136
[2]   A growth factor-dependent nuclear kinase phosphorylates p27Kip1 and regulates cell cycle progression [J].
Boehm, M ;
Yoshimoto, T ;
Crook, MF ;
Nallamshetty, S ;
True, A ;
Nabel, GJ ;
Nabel, EG .
EMBO JOURNAL, 2002, 21 (13) :3390-3401
[3]  
Cao L, 2000, J CELL BIOCHEM, V77, P569, DOI 10.1002/(SICI)1097-4644(20000615)77:4<569::AID-JCB5>3.3.CO
[4]  
2-B
[5]  
Carnero A, 1998, CURR TOP MICROBIOL, V227, P43
[6]   Protein tyrosine phosphatase inhibition induces anti-tumor activity:: Evidence of Cdk2/p27kip1 and Cdk2/SHP-1 complex formation in human ovarian cancer cells [J].
Caron, Danielle ;
Savard, Pierre E. ;
Doillon, Charles J. ;
Olivier, Martin ;
Shink, Eric ;
Lussier, Jacques G. ;
Faure, Robert L. .
CANCER LETTERS, 2008, 262 (02) :265-275
[7]   Genetic Characterization of the Role of the Cip/Kip Family of Proteins as Cyclin-Dependent Kinase Inhibitors and Assembly Factors [J].
Cerqueira, Antonio ;
Martin, Alberto ;
Symonds, Catherine E. ;
Odajima, Junko ;
Dubus, Pierre ;
Barbacid, Mariano ;
Santamaria, David .
MOLECULAR AND CELLULAR BIOLOGY, 2014, 34 (08) :1452-1459
[8]   A cyclin-dependent kinase inhibitor, dacapo, is necessary for timely exit from the cell cycle during Drosophila embryogenesis [J].
deNooij, JC ;
Letendre, MA ;
Hariharan, IK .
CELL, 1996, 87 (07) :1237-1247
[9]  
Groeger AM, 2000, ANTICANCER RES, V20, P3301
[10]  
Hamamoto Hiroshi, 2014, Seikagaku, V86, P578