一种来自斑翅虫雄性生殖道的精子活化胰蛋白酶样蛋白酶:蛋白质组鉴定、序列表征、基因表达谱、RNAi 和电离辐射的影响。

IF 2.3 2区 农林科学 Q1 ENTOMOLOGY Journal of insect physiology Pub Date : 2024-06-17 DOI:10.1016/j.jinsphys.2024.104664
Priya Yadav , Rakesh K. Seth , Stuart E. Reynolds
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引用次数: 0

摘要

与其他鳞翅目昆虫一样,烟草切割蛾(Spodoptera litura)的雄性也会产生两种精子,一种是有核(eupyrene)精子,另一种是无核(apyrene)精子。这两种精子都在睾丸中形成,以未成熟的形式释放到雄性生殖道中,并储存在生殖道的二叠区。这两种精子在这一阶段都没有运动能力。在体外用男性生殖道前列腺区提取物或哺乳动物胰蛋白酶处理储存在双重区的芘精子时,它们会变得有活力;提取物或酶的浓度越高,激活效果越大,速度越快。前列腺提取物的激活作用会被大豆胰蛋白酶抑制剂(SBTI)阻断,这种阻断也是剂量依赖性的。这些结果表明,正常的精子激活过程是由前列腺区域产生的内源性胰蛋白酶样蛋白酶引起的。对S. litura前列腺提取物的蛋白质组分析发现了一种分子量为27 kDa的类胰蛋白酶丝氨酸蛋白酶(TLSP),其199个氨基酸序列与S. litura基因组中的一种预测蛋白相同,并且与其他几种夜蛾物种基因组中基因编码的预测蛋白高度相似。令人惊讶的是,TLSP 与丝蛾的丝氨酸蛋白酶 2(initiatorin)只有很远的亲缘关系,而丝蛾的丝氨酸蛋白酶 2 是迄今为止发现的唯一能激活精子的鳞翅目昆虫蛋白。从前列腺区域提取的总 RNA 合成了 cDNA,并用 qPCR 检测 TLSP 的表达。向成年雄性动物注射 TLSP 特异性 dsRNA 24 小时后,这两个部位的 tlsp mRNA 水平均显著下降。在 10% 的蜂蜜溶液中注射 TLSP dsRNA 的成年雄虫交配的雌虫产卵数量和卵的受精率(孵化率)均有所下降。与对照组相比,给蛹注射 TLSP dsRNA 会显著降低成年雄性前列腺提取物对芘精子活力的激活作用。将 S. litura 蛹暴露于电离辐射中会显著降低辐照雄性前列腺部分和附属腺体中 tlsp mRNA 的表达,无论是在辐照一代还是在其 F1 后代(未受辐照)中都是如此。本文讨论了这些发现对利用遗传不育技术控制 S. litura 和其他有害鳞翅目昆虫的影响。
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A sperm-activating trypsin-like protease from the male reproductive tract of Spodoptera litura: Proteomic identification, sequence characterization, gene expression profile, RNAi and the effects of ionizing radiation

Like other lepidopteran insects, males of the tobacco cutworm moth, Spodoptera litura produce two kinds of spermatozoa, eupyrene (nucleate) and apyrene (anucleate) sperm. Formed in the testis, both kinds of sperm are released into the male reproductive tract in an immature form and are stored in the duplex region of the tract. Neither type of sperm is motile at this stage. When stored apyrene sperm from the duplex are treated in vitro with an extract of the prostatic region of the male tract, or with mammalian trypsin, they become motile; activation is greater and achieved more rapidly with increasing concentration of extract or enzyme. The activating effect of prostatic extract is blocked by soybean trypsin inhibitor (SBTI), also in a dose-dependent way. These results suggest that the normal sperm-activating process is due to an endogenous trypsin-like protease produced in the prostatic region.

Proteomic analysis of S. litura prostatic extracts revealed a Trypsin-Like Serine Protease, TLSP, molecular weight 27 kDa, whose 199-residue amino acid sequence is identical to that of a predicted protein from the S. litura genome and is highly similar to predicted proteins encoded by genes in the genomes of several other noctuid moth species. Surprisingly, TLSP is only distantly related to Serine Protease 2 (initiatorin) of the silkmoth, Bombyx mori, the only identified lepidopteran protein so far shown to activate sperm. TLSP has features typical of secreted proteins, probably being synthesized as an inactive precursor zymogen, which is later activated by proteolytic cleavage.

cDNA was synthesized from total RNA extracted from the prostatic region and was used to examine TLSP expression using qPCR. tlsp mRNA was expressed in both the prostatic region and the accessory glands of the male tract. Injection of TLSP-specific dsRNA into adult males caused a significant reduction after 24 h in tlsp mRNA levels in both locations. The number of eggs laid by females mated to adult males that were given TLSP dsRNA in 10 % honey solution, and the fertility (% hatched) of the eggs were reduced. Injecting pupae with TLSP dsRNA caused the later activation of apyrene sperm motility by adult male prostatic extracts to be significantly reduced compared to controls.

Exposure of S. litura pupae to ionizing radiation significantly reduced expression of tlsp mRNA in the prostatic part and accessory gland of irradiated males in both the irradiated generation and also in their (unirradiated) F1 progeny. The implications of these findings for the use of the inherited sterility technique for the control of S. litura and other pest Lepidoptera are discussed.

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来源期刊
Journal of insect physiology
Journal of insect physiology 生物-昆虫学
CiteScore
4.50
自引率
4.50%
发文量
77
审稿时长
57 days
期刊介绍: All aspects of insect physiology are published in this journal which will also accept papers on the physiology of other arthropods, if the referees consider the work to be of general interest. The coverage includes endocrinology (in relation to moulting, reproduction and metabolism), pheromones, neurobiology (cellular, integrative and developmental), physiological pharmacology, nutrition (food selection, digestion and absorption), homeostasis, excretion, reproduction and behaviour. Papers covering functional genomics and molecular approaches to physiological problems will also be included. Communications on structure and applied entomology can be published if the subject matter has an explicit bearing on the physiology of arthropods. Review articles and novel method papers are also welcomed.
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