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Identification and
characterization of Bms3a in Bombyx mori L.
Xu Jia-Ping1,
Chen Ke-Ping2*, Liu Ming-Hui3, Yao Qin2,
Gao Gui-Tian2 and Zhao Yuan2
1Department
of Life Sciences, Anhui Agricultrual University, 130#
Changjiang western Road, Hefei, 230036, P.R. China.
2Institute
of Life Sciences, Jiangsu University, 301 Xuefu Road,
Zhenjiang 212013, P. R. China.
3Institute
of Sericulture, Anhui Academy of Agricult1ural Sciences,
Hefei 230061, P. R. China.
*Corresponding author. E-mail:
kpchen@ujs.edu.cn.
Accepted
15 August, 2008 |
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Using
fluorescent differential display (FDD) technique, we
analyzed the differential expression of genes related to
BmNPV resistance in highly resistant silkworm strain NB,
highly susceptible silkworm strain 306 and near isogenic
line 306NNZZ. Based on the differential display bands, a 609
bp fragment named C18609 was cloned and confirmed
by Northern blot hybridization. The sequence was then
electric extended by identified in NCBI ESTs. A novel gene
was characterized and revealed to encode a putative BmS3a
protein. Becasue it has high homology to some insect S3a
protein, it was named s3a. S3a protein have been known to
play crucial roles in protein synthesis, and is related to
apoptosis. It is differentially expressed in silkworm high
resistance strain, high susceptible strain and BmNPV treated
silkworms. Therefore, it is conceivable that BmS3a is
involved in silkworm BmNPV resistance.
Key
words:
BmNPV, Resistance, Bms3a, fluorescent differential display. |