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QTL analysis of cocoon shell weight identifies BmRPL18 associated with silk protein synthesis in silkworm by pooling sequencing

机译:茧壳重量的QTL分析通过池测序确定蚕中蚕丝蛋白合成相关的BmRPL18

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摘要

Mechanisms that regulate silk protein synthesis provide the basis for silkworm variety breeding and silk gland bioreactor optimization. Here, using the pooling sequencing-based methodology, we deciphered the genetic basis for the varied silk production in different silkworm strains. We identified 8 SNPs, with 6 on chromosome 11 and 1 each on chromosomes 22 and 23, that were linked with silk production. After conducting an association analysis between gene expression pattern, silk gland development and cocoon shell weight (CSW), BMGN011620 was found to be regulating silk production. BMGN011620 encodes the 60S ribosomal protein, L18, which is an indispensable component of the 60S ribosomal subunit; therefore we named it BmRPL18. Moreover, the clustering of linked SNPs on chromosome 11 and the analysis of differentially expressed genes reported in previous Omics studies indicated that the genes regulating silk protein synthesis may exhibit a clustering distribution in the silkworm genome. These results collectively advance our understanding of the regulation of silk production, including the role of ribosomal proteins and the clustered distribution of genes involved in silk protein synthesis.
机译:调节丝蛋白合成的机制为家蚕品种育种和丝腺生物反应器优化提供了基础。在这里,使用基于合并测序的方法,我们破译了不同蚕品系中不同的蚕丝生产的遗传基础。我们鉴定了8​​个SNP,其中11个染色体上有6个,而22和23号染色体上各有1个,它们与丝绸的生产有关。在对基因表达模式,丝腺发育和茧壳重量(CSW)之间进行关联分析后,发现BMGN011620调节着丝的产量。 BMGN011620编码60S核糖体蛋白L18,它是60S核糖体亚基必不可少的成分。因此我们将其命名为BmRPL18。此外,在11号染色体上连接的SNP的聚类以及先前Omics研究中报道的差异表达基因的分析表明,调节蚕丝蛋白合成的基因可能在蚕基因组中表现出聚类分布。这些结果共同推动了我们对丝生产调节的理解,包括核糖体蛋白的作用以及参与丝蛋白合成的基因的聚集分布。

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