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Cloning and Expression Characteristics of the Notch-Associated Gene BmE( spl) mγ from Silkworm, Bombyx mori.

Authors :
Liu, Min
Wang, Chan
Li, Dan
Liu, Yue
Sheng, Qing
Lv, Zhengbing
Yu, Wei
Wang, Dan
Zhang, Yaozhou
Nie, Zuoming
Source :
Applied Biochemistry & Biotechnology; Aug2014, Vol. 173 Issue 8, p2065-2075, 11p
Publication Year :
2014

Abstract

The E( spl) mγ gene in Drosophila is a regulatory target gene downstream of the Notch pathway. BmE( spl) mγ ( Bombyx mori, E( spl) mγ) is an ortholog of the Drosophila E( spl) mγ gene, and the gene encodes a protein with 248 amino acid residues. This gene was cloned and overexpressed in Escherichia coli BL21(DE3). The recombinant protein was purified and subsequently used to generate a rabbit polyclonal antibody. Western blotting analyses showed that BmE( spl) mγ expression is high in pupa and egg, and low in larva and moth. In the fifth instar larva, the protein levels are high in head, epidermis, sexual gland, trachea, and the fatbody and low in the Malpighian tubule, hemolymph, gut, and silk gland. The further immunohistochemical analyses also showed higher BmE( spl) mγ expression in the head of fifth instar larva and pupa. Of the four moth parts studied, the thorax had the highest expression level. Thus, BmE(spl)mγ might be associated with neurogenesis in silkworm. Furthermore, DAPT (a γ-secretase inhibitor and an indirect inhibitor of Notch) blocking experiments showed that higher concentrations of the blocking agent and a longer processing time reduce the transcription levels of the BmE( spl) mγ gene, demonstrating that the silkworm BmE( spl) mγ gene is associated with the Notch signal pathway. These findings suggest that the function of BmE( spl) mγ may be similar to that of its Drosophila homolog. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02732289
Volume :
173
Issue :
8
Database :
Complementary Index
Journal :
Applied Biochemistry & Biotechnology
Publication Type :
Academic Journal
Accession number :
97460708
Full Text :
https://doi.org/10.1007/s12010-014-1003-2