Bmovo-1 regulates ovary size in the silkworm, Bombyx mori

PLoS One. 2014 Aug 13;9(8):e104928. doi: 10.1371/journal.pone.0104928. eCollection 2014.

Abstract

The regulation of antagonistic OVO isoforms is critical for germline formation and differentiation in Drosophila. However, little is known about genes related to ovary development. In this study, we cloned the Bombyx mori ovo gene and investigated its four alternatively spliced isoforms. BmOVO-1, BmOVO-2 and BmOVO-3 all had four C2H2 type zinc fingers, but differed at the N-terminal ends, while BmOVO-4 had a single zinc finger. Bmovo-1, Bmovo-2 and Bmovo-4 showed the highest levels of mRNA in ovaries, while Bmovo-3 was primarily expressed in testes. The mRNA expression pattern suggested that Bmovo expression was related to ovary development. RNAi and transgenic techniques were used to analyze the biological function of Bmovo. The results showed that when the Bmovo gene was downregulated, oviposition number decreased. Upregulation of Bmovo-1 in the gonads of transgenic silkworms increased oviposition number and elevated the trehalose contents of hemolymph and ovaries. We concluded that Bmovo-1 was involved in protein synthesis, contributing to the development of ovaries and oviposition number in silkworms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified / anatomy & histology
  • Animals, Genetically Modified / genetics
  • Animals, Genetically Modified / growth & development
  • Animals, Genetically Modified / metabolism
  • Bombyx / anatomy & histology
  • Bombyx / genetics*
  • Bombyx / growth & development*
  • Bombyx / metabolism
  • Female
  • Insect Proteins / analysis
  • Insect Proteins / genetics*
  • Insect Proteins / metabolism
  • Organ Size
  • Ovary / anatomy & histology
  • Ovary / growth & development
  • Ovary / metabolism
  • Oviposition
  • Protein Isoforms / analysis
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Up-Regulation

Substances

  • Insect Proteins
  • Protein Isoforms

Grants and funding

We gratefully acknowledge the financial support of the National Basic Research Program of China (973 Program, 2012CB114600), the National Natural Science Foundation of China (31072085), the Specialized Research Fund for the Doctoral Program of Higher Education (20113201130002), and a project funded by the Priority Academic Program of Development of Jiangsu Higher Education Institutions. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.