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舞毒蛾触角发育过程中信息素结合蛋白的表达

Expression of pheromone binding proteins during antennal development in the gypsy moth Lymantria dispar.

作者信息

Vogt R G, Köhne A C, Dubnau J T, Prestwich G D

机构信息

Department of Chemistry, State University of New York, Stony Brook 11794.

出版信息

J Neurosci. 1989 Sep;9(9):3332-46. doi: 10.1523/JNEUROSCI.09-09-03332.1989.

Abstract

We have identified 2 olfactory specific proteins in the gypsy moth Lymantria dispar that are uniquely associated with the male antennae, the principal olfactory organs of this animal. These proteins were the major soluble protein components of the olfactory sensilla, present in equivalent amounts. Both proteins comigrated on SDS-PAGE, showing an apparent molecular mass of 15,000 Da but migrated separately on non-SDS-PAGE, indicating differences in net charge. N-terminal amino acid sequence analysis showed that the 2 proteins share 50% identity, indicating that they are genetically distinct homologs. Both proteins bound the L. dispar sexpheromone, associated with antisera prepared against the previously identified phermone-binding protein (PBP) of the moth Antheraea polyphemus, and shared sequence identity with the A. polyphemus PBP. These 2 proteins are therefore identified as L. dispar PBPs and are termed PBP1 and PBP2 based on their migration differences on non-SDS-PAGE. It is estimated that PBP1 and PBP2 are present in the sensilla lumen at a combined concentration of 13.4 mM. The expression of the L. dispar PBPs was examined during the 11 d development of the adult antenna. PBP1 and PBP2 were first detected by non-SDS-PAGE analysis and Coomassie blue staining 3 d before adult eclosion, on day A-3. Levels increased, reaching a plateau on day A-1 that continued into adult life. In vivo labeling studies indicated that the rate of PBP synthesis increased from A-3 to a plateau on A-2, where it remained into adult life. In vitro translations of antennal mRNAs indicated that translatable PBP mRNA was available at a very low level on day A-4, increased slightly on A-3 and dramatically on A-2, and remained at a high level into adult life. PBP mRNA represented the major translatable mRNA in the antenna during this period. It was estimated that the PBPs undergo a combined steady-state turnover of 8 x 10(7) molecules/hr/sensillum. Cursory in vivo and in vitro translation studies of antennal mRNA from A. polyphemus and Manduca sexta showed similar temporal patterns of PBP expression, suggesting that the L. dispar observations are general.

摘要

我们在舞毒蛾中鉴定出了2种嗅觉特异性蛋白,它们与雄性触角(该动物的主要嗅觉器官)独特相关。这些蛋白是嗅觉感受器的主要可溶性蛋白成分,含量相当。两种蛋白在SDS-PAGE上共迁移,显示表观分子量为15,000 Da,但在非SDS-PAGE上分别迁移,表明净电荷存在差异。N端氨基酸序列分析表明,这两种蛋白有50%的同源性,表明它们是基因上不同的同源物。两种蛋白都能结合舞毒蛾性信息素,与针对先前鉴定的多音柞蚕信息素结合蛋白(PBP)制备的抗血清相关,并且与多音柞蚕PBP有序列同源性。因此,这两种蛋白被鉴定为舞毒蛾PBP,并根据它们在非SDS-PAGE上的迁移差异分别称为PBP1和PBP2。据估计,PBP1和PBP2在感受器管腔中的总浓度为13.4 mM。在成虫触角11天的发育过程中检测了舞毒蛾PBP的表达。在成虫羽化前3天,即A-3天,通过非SDS-PAGE分析和考马斯亮蓝染色首次检测到PBP1和PBP2。其水平升高,在A-1天达到平台期并持续到成虫期。体内标记研究表明,PBP合成速率从A-3天增加到A-2天的平台期,并在成虫期保持该水平。触角mRNA的体外翻译表明,在A-4天可翻译的PBP mRNA水平非常低,在A-3天略有增加,在A-2天显著增加,并在成虫期保持在高水平。在此期间,PBP mRNA是触角中主要的可翻译mRNA。据估计,PBP的稳态周转总量为8×10⁷个分子/小时/感受器。对多音柞蚕和烟草天蛾触角mRNA进行的初步体内和体外翻译研究显示,PBP表达具有相似的时间模式,表明舞毒蛾的观察结果具有普遍性。

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