Literature DB >> 28379781

Two Geminin homologs regulate DNA replication in silkworm, Bombyx mori.

Xiao-Fang Tang1, Xiang-Yun Chen1,2, Chun-Dong Zhang1,3, Yao-Feng Li1,2, Tai-Hang Liu1, Xiao-Lin Zhou1, Qian Zhang1, Peng Chen1,4, Cheng Lu1,4, Min-Hui Pan1,4.   

Abstract

DNA replication is rigorously controlled in cells to ensure that the genome duplicates exactly once per cell cycle. Geminin is a small nucleoprotein, which prevents DNA rereplication by directly binding to and inhibiting the DNA replication licensing factor, Cdt1. In this study, we have identified 2 Geminin genes, BmGeminin1 and BmGeminn2, in silkworm, Bombyx mori. These genes contain the Geminin conserved coiled-coil domain and are periodically localized in the nucleus during the S-G2 phase but are degraded at anaphase in mitosis. Both BmGeminin1 and BmGeminin2 are able to homodimerize and interact with BmCdt1 in cells. In addition, BmGeminin1 and BmGeminin2 can interact with each other. Overexpression of BmGeminin1 affects cell cycle progression: cell cycle is arrested in S phase, and RNA interference of BmGeminin1 leads to rereplication. In contrast, overexpression or knockdown of BmGeminin2 with RNAi did not significantly affect cell cycle, while more rereplication occurred when BmGeminin1 and BmGeminin2 together were knocked down in cells than when only BmGeminin1 was knocked down. These data suggest that both BmGeminin1 and BmGeminin2 are involved in the regulation of DNA replication. These findings provide insight into the function of Geminin and contribute to our understanding of the regulation mechanism of cell cycle in silkworm.

Entities:  

Keywords:  Bombyx mori; Cdt1; DNA replication; Geminin; cell cycle

Mesh:

Substances:

Year:  2017        PMID: 28379781      PMCID: PMC5444359          DOI: 10.1080/15384101.2017.1282582

Source DB:  PubMed          Journal:  Cell Cycle        ISSN: 1551-4005            Impact factor:   4.534


  40 in total

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4.  Bombyx mori Nucleopolyhedrovirus (BmNPV) Induces G2/M Arrest to Promote Viral Multiplication by Depleting BmCDK1.

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