{"title":"灰鼠科dopa -脱羧酶基因的谱系特异性重复和功能多样化研究","authors":"Shintaro Inoue , Kai Fujie , Taiki Hamaguchi , Yoshiyasu Ishimaru , Katsuyuki Miyawaki , Akira Takahashi , Takeshi Nikawa , Sumihare Noji , Takahito Watanabe , Taro Mito","doi":"10.1016/j.ibmb.2024.104246","DOIUrl":null,"url":null,"abstract":"<div><div>The DOPA-decarboxylase (DDC) gene is crucial for dopamine synthesis and influences various biological functions in insects, including body coloration, behavior, learning, and sleep. However, its evolutionary impact remains largely unexplored. This study reports on the tandem duplication of two <em>bona fide ddc</em> genes (<em>ddc1</em> and <em>ddc2</em>) in the <em>Gryllidae</em> cricket family. We herein investigated the function of <em>ddc1</em> and <em>ddc2</em> using <em>Gryllus bimaculatus</em> (<em>Gb</em>) as a model. Our results revealed that <em>Gb'ddc1</em> was expressed systemically, with its expression being higher immediately after molting compared to the stage following melanin pigmentation. In homozygous knockout mutants of <em>Gb'ddc1</em>, generated via CRISPR/Cas9, reduced body color pigmentation and had translucent cuticles, decreased dopamine levels, and over-accumulated DOPA. These mutants died shortly after hatching, likely due to cuticle defects, underscoring the essential role of dopamine, produced by <em>Gb'ddc1,</em> in melanin synthesis. Conversely, <em>Gb'ddc2</em> expression was confined to the ovary and was not up-regulated after molting. Homozygous knockout mutants of <em>Gb'ddc2</em> exhibited no body color defects, whereas hatchability and embryonic development rates were significantly reduced. Interestingly, dopamine levels in the ovaries were significantly elevated in <em>Gb'ddc2</em> mutants. This suggests that normal ovarian dopamine levels, modulated by <em>Gb'ddc2,</em> are vital for fertility maintenance. The function of <em>Gb'ddc2</em> differs from that of typical <em>ddc</em>, indicating neofunctionalization through evolutionary duplication. Overall, <em>Gb'ddc1</em> and <em>Gb'ddc2</em> have distinct functions, and precise regulation of ovarian dopamine levels using these two <em>ddc</em> genes may have enhanced cricket fertility.</div></div>","PeriodicalId":330,"journal":{"name":"Insect Biochemistry and Molecular Biology","volume":"177 ","pages":"Article 104246"},"PeriodicalIF":3.2000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lineage-specific duplication and functional diversification of DOPA-decarboxylase genes in the Gryllidae family, as revealed in Gryllus bimaculatus\",\"authors\":\"Shintaro Inoue , Kai Fujie , Taiki Hamaguchi , Yoshiyasu Ishimaru , Katsuyuki Miyawaki , Akira Takahashi , Takeshi Nikawa , Sumihare Noji , Takahito Watanabe , Taro Mito\",\"doi\":\"10.1016/j.ibmb.2024.104246\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The DOPA-decarboxylase (DDC) gene is crucial for dopamine synthesis and influences various biological functions in insects, including body coloration, behavior, learning, and sleep. However, its evolutionary impact remains largely unexplored. This study reports on the tandem duplication of two <em>bona fide ddc</em> genes (<em>ddc1</em> and <em>ddc2</em>) in the <em>Gryllidae</em> cricket family. We herein investigated the function of <em>ddc1</em> and <em>ddc2</em> using <em>Gryllus bimaculatus</em> (<em>Gb</em>) as a model. Our results revealed that <em>Gb'ddc1</em> was expressed systemically, with its expression being higher immediately after molting compared to the stage following melanin pigmentation. In homozygous knockout mutants of <em>Gb'ddc1</em>, generated via CRISPR/Cas9, reduced body color pigmentation and had translucent cuticles, decreased dopamine levels, and over-accumulated DOPA. These mutants died shortly after hatching, likely due to cuticle defects, underscoring the essential role of dopamine, produced by <em>Gb'ddc1,</em> in melanin synthesis. Conversely, <em>Gb'ddc2</em> expression was confined to the ovary and was not up-regulated after molting. Homozygous knockout mutants of <em>Gb'ddc2</em> exhibited no body color defects, whereas hatchability and embryonic development rates were significantly reduced. Interestingly, dopamine levels in the ovaries were significantly elevated in <em>Gb'ddc2</em> mutants. This suggests that normal ovarian dopamine levels, modulated by <em>Gb'ddc2,</em> are vital for fertility maintenance. The function of <em>Gb'ddc2</em> differs from that of typical <em>ddc</em>, indicating neofunctionalization through evolutionary duplication. Overall, <em>Gb'ddc1</em> and <em>Gb'ddc2</em> have distinct functions, and precise regulation of ovarian dopamine levels using these two <em>ddc</em> genes may have enhanced cricket fertility.</div></div>\",\"PeriodicalId\":330,\"journal\":{\"name\":\"Insect Biochemistry and Molecular Biology\",\"volume\":\"177 \",\"pages\":\"Article 104246\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Insect Biochemistry and Molecular Biology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0965174824001772\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Insect Biochemistry and Molecular Biology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0965174824001772","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Lineage-specific duplication and functional diversification of DOPA-decarboxylase genes in the Gryllidae family, as revealed in Gryllus bimaculatus
The DOPA-decarboxylase (DDC) gene is crucial for dopamine synthesis and influences various biological functions in insects, including body coloration, behavior, learning, and sleep. However, its evolutionary impact remains largely unexplored. This study reports on the tandem duplication of two bona fide ddc genes (ddc1 and ddc2) in the Gryllidae cricket family. We herein investigated the function of ddc1 and ddc2 using Gryllus bimaculatus (Gb) as a model. Our results revealed that Gb'ddc1 was expressed systemically, with its expression being higher immediately after molting compared to the stage following melanin pigmentation. In homozygous knockout mutants of Gb'ddc1, generated via CRISPR/Cas9, reduced body color pigmentation and had translucent cuticles, decreased dopamine levels, and over-accumulated DOPA. These mutants died shortly after hatching, likely due to cuticle defects, underscoring the essential role of dopamine, produced by Gb'ddc1, in melanin synthesis. Conversely, Gb'ddc2 expression was confined to the ovary and was not up-regulated after molting. Homozygous knockout mutants of Gb'ddc2 exhibited no body color defects, whereas hatchability and embryonic development rates were significantly reduced. Interestingly, dopamine levels in the ovaries were significantly elevated in Gb'ddc2 mutants. This suggests that normal ovarian dopamine levels, modulated by Gb'ddc2, are vital for fertility maintenance. The function of Gb'ddc2 differs from that of typical ddc, indicating neofunctionalization through evolutionary duplication. Overall, Gb'ddc1 and Gb'ddc2 have distinct functions, and precise regulation of ovarian dopamine levels using these two ddc genes may have enhanced cricket fertility.
期刊介绍:
This international journal publishes original contributions and mini-reviews in the fields of insect biochemistry and insect molecular biology. Main areas of interest are neurochemistry, hormone and pheromone biochemistry, enzymes and metabolism, hormone action and gene regulation, gene characterization and structure, pharmacology, immunology and cell and tissue culture. Papers on the biochemistry and molecular biology of other groups of arthropods are published if of general interest to the readership. Technique papers will be considered for publication if they significantly advance the field of insect biochemistry and molecular biology in the opinion of the Editors and Editorial Board.