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舞毒蛾(鳞翅目:夜蛾科)性别决定基因的鉴定与功能分析

Identification and functional analysis of sex-determining genes in the spongy moth, Lymantria dispar (lepidoptera: Erebidae).

作者信息

Moronuki Yuto, Kasahara Ryota, Naka Hideshi, Suzuki Masataka G

机构信息

Department of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, 277-8562, Chiba, Japan.

Department of Research for Parkinson's Disease & Center for Genomic and Regenerative Medicine, Graduate School of Medicine, Juntendo University, 113-8421, Tokyo, Japan.

出版信息

Insect Biochem Mol Biol. 2025 Feb;177:104219. doi: 10.1016/j.ibmb.2024.104219. Epub 2024 Nov 22.

Abstract

The spongy moth (Lymantria dispar) employs a female heterogametic sex-determination system, where the female sex-determining factor (F factor) is located on the W chromosome, and the male sex-determining factor (M factor) is located on the Z chromosome. The sex-determining capabilities of the F factor and M factor vary among subspecies. Consequently, L. dispar serves as an excellent model for studying the mechanisms underlying the evolution and diversity of sex-determining genes. However, the genes encoding the F and M factors, as well as the molecular functions of their translation products, remain unidentified. In this study, we identified a L. dispar Masculinizer ortholog (LdMasc) and found that this gene is highly expressed in male embryos during the sex-determination stage. When LdMasc expression was silenced using embryonic RNA interference (RNAi), the expression pattern of L. dispar doublesex (Lddsx), the master regulatory gene for sex differentiation, shifted from the male-specific form to the female-specific form in male embryos. To identify potential F factors, we screened for genes that were exclusively expressed in females across multiple tissues and located only within the female genome. This screening yielded four unigenes with sequences displaying high homology to each other. These unigenes formed a tandem repeat, comprising approximately 100 copies within a 200 kbp region of the W chromosome-derived contig. We designated these unigenes as Fet-W (female-specifically expressed transcript from the W chromosome). RT-PCR analysis revealed that Fet-W was expressed in a female-specific manner during the sex-determination stage. Suppression of Fet-W expression by embryonic RNAi led to an increase in LdMasc expression in females and a corresponding shift in dsx expression patterns from the female-specific to the male-specific form. These findings strongly suggest that the F factor in L. dispar is Fet-W, whereas the M factor is LdMasc.

摘要

舞毒蛾(Lymantria dispar)采用雌性异配性别决定系统,其中雌性性别决定因子(F因子)位于W染色体上,而雄性性别决定因子(M因子)位于Z染色体上。F因子和M因子的性别决定能力在不同亚种间有所差异。因此,舞毒蛾是研究性别决定基因进化和多样性潜在机制的优秀模型。然而,编码F因子和M因子的基因及其翻译产物的分子功能仍未明确。在本研究中,我们鉴定出一个舞毒蛾雄性化因子直系同源物(LdMasc),并发现该基因在性别决定阶段的雄性胚胎中高度表达。当使用胚胎RNA干扰(RNAi)使LdMasc表达沉默时,性别分化的主要调控基因——舞毒蛾双性基因(Lddsx)在雄性胚胎中的表达模式从雄性特异性形式转变为雌性特异性形式。为了鉴定潜在的F因子,我们筛选了在多个组织中仅在雌性中表达且仅位于雌性基因组内的基因。该筛选产生了四个彼此序列显示高度同源性的单基因。这些单基因形成一个串联重复,在源自W染色体的重叠群的200 kbp区域内包含约100个拷贝。我们将这些单基因命名为Fet-W(来自W染色体的雌性特异性表达转录本)。逆转录聚合酶链反应(RT-PCR)分析表明,Fet-W在性别决定阶段以雌性特异性方式表达。通过胚胎RNAi抑制Fet-W表达导致雌性中LdMasc表达增加,并且dsx表达模式相应地从雌性特异性形式转变为雄性特异性形式。这些发现有力地表明,舞毒蛾中的F因子是Fet-W,而M因子是LdMasc。

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