首页> 外文期刊>Journal of proteome research >Mitochondrial proteins differential expression during honeybee (Apis mellifera L.) queen and worker larvae caste determination
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Mitochondrial proteins differential expression during honeybee (Apis mellifera L.) queen and worker larvae caste determination

机译:蜜蜂(Apis mellifera L.)女王和工人幼虫种姓测定过程中线粒体蛋白的差异表达

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Despite their similar genetic makeup, honeybee (A. mellifera) queens and workers show alternative morphologies driven by nutritional difference during the larval stage. Although much research have been done to investigate the causes of honeybee caste polymorphism, information at subcellular protein levels is limited. We analyzed queen- and worker-destined larvae mitochondrial proteome at three early developmental stages using combinations of differential centrifugation, two-dimensional electrophoresis, mass spectrometry, bioinformatics, and quantitative real time PCR. In total, 67, 69, and 97 protein spots were reproducibly identified as mitochondrial proteins at 72, 96, and 120 h, respectively. There were significant qualitative and quantitative protein expression differences between the two castes at three developmental stages. In general, the queen-destined larvae up-regulated large proportions of proteins at all of the developmental stages and, in particular, 95% at 72 h. An overwhelming majority of the queen larvae up-regulated proteins were physiometabolic-enriched proteins (metabolism of carbohydrate and energy, amino acid, and fatty acid) and involved in protein folding, and this was further verified by functional enrichment and biological interaction network analyses as a direct link with metabolic rates and cellular responses to hormones. Although wide-ranging mitochondrial proteomes participate to shape the metabolic, physiologic, and anatomic differences between the two castes at 72 h, physiometabolic-enriched proteins were found as the major modulators of the profound marking of this caste differentiation. Owing to nutritional difference, prospective queen larvae showed enhanced growth, and this was manifested through the overexpression of metabolic enzymes. Differently from similar studies targeting the causes of honeybee caste polymorphism, this subcellular level study provides an in-depth insight into mitochondrial proteins-mediated caste polymorphism and greatly improves protein coverage involved during honeybee caste determination. Hence, it is a major step forward in the analysis of the fundamental causes of honeybee caste pathway decision and greatly contributes to the knowledge of honeybee biology. In particular, the consistency between the 22 proteins and mRNA expressions provides us important target genes for the reverse genetic analysis of caste pathway modulation through RNA interference.
机译:尽管它们的基因组成相似,但蜜蜂(A. mellifera)的皇后和工人在幼虫期表现出受营养差异驱动的其他形态。尽管已经进行了大量研究来调查蜜蜂种姓多态性的原因,但是亚细胞蛋白水平的信息仍然有限。我们使用差速离心,二维电泳,质谱,生物信息学和定量实时PCR的组合,在三个早期的发育阶段分析了皇后区和工人定居的幼虫线粒体蛋白质组。总共可分别在72、96和120 h将67、69和97个蛋白斑点鉴定为线粒体蛋白。在三个发育阶段,两个种姓之间存在明显的定性和定量蛋白质表达差异。通常,在所有发育阶段,皇后定居的幼虫上调大部分蛋白质,特别是在72小时时上调95%。绝大多数的皇后幼虫上调蛋白质是富含代谢代谢的蛋白质(碳水化合物,能量,氨基酸和脂肪酸的代谢)并参与蛋白质折叠,并且通过功能富集和生物学相互作用网络分析进一步证实了这一点。与代谢率和细胞对激素的反应直接相关。尽管广泛的线粒体蛋白质组参与在72 h塑造两个种姓之间的代谢,生理和解剖差异,但发现富含代谢代谢产物的蛋白质是这种种姓分化深刻标志的主要调节剂。由于营养上的差异,准皇后幼虫显示出增强的生长,这通过代谢酶的过表达得以体现。与针对蜜蜂种姓多态性成因的类似研究不同,该亚细胞水平研究提供了对线粒体蛋白质介导的种姓多态性的深入了解,并极大地提高了蜜蜂种姓测定过程中涉及的蛋白质覆盖率。因此,这是在分析蜜蜂种姓途径决定的根本原因方面迈出的重要一步,并极大地促进了蜜蜂生物学的知识。特别地,22种蛋白质和mRNA表达之间的一致性为我们通过RNA干扰进行种姓途径调控的反向遗传分析提供了重要的靶基因。

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