The Expression, Purification, and Characterization of a Ras Oncogene (Bras2) in Silkworm (Bombyx mori)

Bibliographic Details
Title: The Expression, Purification, and Characterization of a Ras Oncogene (Bras2) in Silkworm (Bombyx mori)
Authors: Zhengbing Lv, Tao Wang, Wenhua Zhuang, Dan Wang, Jian Chen, Zuoming Nie, Lili Liu, Wenping Zhang, Lisha Wang, Deming Wang, Xiangfu Wu, Jun Li, Lian Qian, Yaozhou Zhang
Source: International Journal of Genomics, Vol 2013 (2013)
Publisher Information: Hindawi Limited, 2013.
Publication Year: 2013
Collection: LCC:Genetics
Subject Terms: Genetics, QH426-470
More Details: The Ras oncogene of silkworm pupae (Bras2) may belong to the Ras superfamily. It shares 77% of its amino acid identity with teratocarcinoma oncogene 21 (TC21) related ras viral oncogene homolog-2 (R-Ras2) and possesses an identical core effector region. The mRNA of Bombyx mori Bras2 has 1412 bp. The open reading frame contains 603 bp, which encodes 200 amino acid residues. This recombinant BmBras2 protein was subsequently used as an antigen to raise a rabbit polyclonal antibody. Western blotting and real-time PCR analyses showed that BmBras2 was expressed during four developmental stages. The BmBras2 expression level was the highest in the pupae and was low in other life cycle stages. BmBras2 was expressed in all eight tested tissues, and it was highly expressed in the head, intestine, and epidermis. Subcellular localization studies indicated that BmBras2 was predominantly localized in the nuclei of Bm5 cells, although cytoplasmic staining was also observed to a lesser extent. A cell proliferation assay showed that rBmBras2 could stimulate the proliferation of hepatoma cells. The higher BmBras2 expression levels in the pupal stage, tissue expression patterns, and a cell proliferation assay indicated that BmBras2 promotes cell division and proliferation, most likely by influencing cell signal transduction.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2314-436X
2314-4378
Relation: https://doaj.org/toc/2314-436X; https://doaj.org/toc/2314-4378
DOI: 10.1155/2013/269609
Access URL: https://doaj.org/article/b0c0ff9c91e14afb850e4399027e268c
Accession Number: edsdoj.b0c0ff9c91e14afb850e4399027e268c
Database: Directory of Open Access Journals
More Details
ISSN:2314436X
23144378
DOI:10.1155/2013/269609
Published in:International Journal of Genomics
Language:English