蚕业科学
蠶業科學
잠업과학
ACTA SERICOLOGICA SINICA
2009年
4期
754-760
,共7页
钱平%吴阳春%柴春利%代方银%鲁成
錢平%吳暘春%柴春利%代方銀%魯成
전평%오양춘%시춘리%대방은%로성
家蚕%胚胎发育%体节极性基因%基因克隆%序列分析%表达模式
傢蠶%胚胎髮育%體節極性基因%基因剋隆%序列分析%錶達模式
가잠%배태발육%체절겁성기인%기인극륭%서렬분석%표체모식
Bombyx mori%Embryonic development%Decapentaplegic gene dpp%Gene cloning%Sequence analysis%Expression pattern
体节极性基因dpp是昆虫发育过程中的关键基因.采用生物信息学的方法,利用家蚕EST数据获得了家蚕dpp基因(Bmdpp)cDNA序列.该cDNA序列全长1 206 bp,ORF 1 146 bp,编码381个氨基酸,预测蛋白分子质量38.6 kD,等电点9.18.将克隆的Bmdpp基因完整CDS序列亚克隆到pET-28a(+)表达载体,转化、诱导后经SDS-PAGE电泳检测到约40 kD与预测分子质量相符的目的蛋白条带.对Bmdpp在家蚕胚胎不同发育时期的表达分析发现,该基因在受精6~14 h的表达量很低,甚至没有表达.这一表达模式和果蝇dpp基因在胚胎发育过程中的表达模式相似,推测Bmdpp在家蚕早期胚胎发育的背-腹轴分化中起作用.
體節極性基因dpp是昆蟲髮育過程中的關鍵基因.採用生物信息學的方法,利用傢蠶EST數據穫得瞭傢蠶dpp基因(Bmdpp)cDNA序列.該cDNA序列全長1 206 bp,ORF 1 146 bp,編碼381箇氨基痠,預測蛋白分子質量38.6 kD,等電點9.18.將剋隆的Bmdpp基因完整CDS序列亞剋隆到pET-28a(+)錶達載體,轉化、誘導後經SDS-PAGE電泳檢測到約40 kD與預測分子質量相符的目的蛋白條帶.對Bmdpp在傢蠶胚胎不同髮育時期的錶達分析髮現,該基因在受精6~14 h的錶達量很低,甚至沒有錶達.這一錶達模式和果蠅dpp基因在胚胎髮育過程中的錶達模式相似,推測Bmdpp在傢蠶早期胚胎髮育的揹-腹軸分化中起作用.
체절겁성기인dpp시곤충발육과정중적관건기인.채용생물신식학적방법,이용가잠EST수거획득료가잠dpp기인(Bmdpp)cDNA서렬.해cDNA서렬전장1 206 bp,ORF 1 146 bp,편마381개안기산,예측단백분자질량38.6 kD,등전점9.18.장극륭적Bmdpp기인완정CDS서렬아극륭도pET-28a(+)표체재체,전화、유도후경SDS-PAGE전영검측도약40 kD여예측분자질량상부적목적단백조대.대Bmdpp재가잠배태불동발육시기적표체분석발현,해기인재수정6~14 h적표체량흔저,심지몰유표체.저일표체모식화과승dpp기인재배태발육과정중적표체모식상사,추측Bmdpp재가잠조기배태발육적배-복축분화중기작용.
Decapentaplegic gene dpp is essential in the embryonic development of insects. By means of bioinformatics, the silkworm (Bombyx mori) EST database was utilized to obtain cDNA sequence of the silkworm dpp gene designated as Bmdpp. The full-length cDNA sequence was 1 206 bp in size, which comprised an open reading frame of 1 146 bp and coded for a protein of 381 amino acid residues. The deduced molecular weight was 38.6 kD and pI 9.18. After the complete coding sequence of cloned Bmdpp gene was subcloned into expression vector pET-28a( + ) by transformation and was induced to express, a target protein band about 40 kD was detected in SDS-PAGE electrophoresis, which was consistent with the predicted molecular weight. Expression analyses of Bmdpp gene at different developmental stages indicated that there was very low level or even no expression during 6 to 14 hours after fertilization. This expression pattern was similar to that of Drosophila dpp gene during embryonic development. It was thus speculated that Bmdpp played a role in dorsal-ventral axis differentiation in early embryonic development of silkworm.