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转录组分析为菲律宾培育的杂交种杂种优势的分子基础提供了见解。

Transcriptomic Profiling Provides Insight into the Molecular Basis of Heterosis in Philippine-Reared Hybrids.

作者信息

Conde Ma Ysabella Elaine D, Planta Jose, Bautista Ma Anita M

机构信息

National Institute of Molecular Biology and Biotechnology, University of the Philippines Diliman, Quezon City 1101, Philippines.

出版信息

Insects. 2025 Feb 26;16(3):243. doi: 10.3390/insects16030243.

Abstract

In the Philippines, parental strains Lat21 and B221 are crossed to yield NC144 and CN144, which demonstrate hybrid vigor. The molecular basis of the observed vigor in the hybrids is warranted, as it may assist in improving local sericulture programs. This study, therefore, aims to investigate the basis of hybrid vigor and generate molecular resources through whole-silkworm larvae transcriptome sequencing, assembly, and analysis. Differential gene expression was also conducted among the parental strains and hybrids. Assembly of the pre-processed reads was also performed using de novo and reference-based protocols. As expected, the reference-based assembly was better than de novo, based on E90N50, N50, and BUSCO assembly completeness metrics. The Analysis of the differentially expressed genes (DEGs) revealed 202 upregulated and 182 downregulated genes in the hybrids (with the parents as the reference) and 66 upregulated and 753 downregulated genes in NC144 (with CN144 as the reference). Among these were genes encoding heat shock proteins and antimicrobial peptides, which may serve as markers for marker-assisted breeding. The genes were further validated using quantitative real-time PCR. Moreover, the inducible nature of these genes under stressors like extreme temperature and bacterial exposure suggests their potential as diagnostic tools for stress assessment.

摘要

在菲律宾,亲本品系Lat21和B221杂交产生了NC144和CN144,它们表现出杂种优势。鉴于杂种优势可能有助于改进当地的养蚕计划,因此有必要研究观察到的杂种优势的分子基础。因此,本研究旨在通过全蚕幼虫转录组测序、组装和分析来探究杂种优势的基础并生成分子资源。同时也对亲本品系和杂种进行了差异基因表达分析。还使用从头组装和基于参考的协议对预处理后的reads进行了组装。正如预期的那样,基于E90N50、N50和BUSCO组装完整性指标,基于参考的组装比从头组装更好。对差异表达基因(DEG)的分析显示,杂种中有202个上调基因和182个下调基因(以亲本为参考),在NC144中有66个上调基因和753个下调基因(以CN144为参考)。其中包括编码热休克蛋白和抗菌肽的基因,这些基因可用作分子标记辅助育种的标记。这些基因通过定量实时PCR进一步验证。此外,这些基因在极端温度和细菌暴露等应激源下的可诱导性表明它们有潜力作为应激评估的诊断工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdc8/11942671/079c53dded57/insects-16-00243-g001.jpg

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