Ultrabithorax is essential for bacteriocyte development

Symbiosis often entails the emergence of novel adaptive traits in organisms. Microbial symbionts are indispensable for diverse insects via provisioning of essential nutrients, wherein novel host cells and organs for harboring the microbes, called bacteriocytes and bacteriomes, have evolved repeatedl...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2015-07, Vol.112 (30), p.9376-9381
Hauptverfasser: Matsuura, Yu, Yoshitomo Kikuchi, Toru Miura, Takema Fukatsu
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creator Matsuura, Yu
Yoshitomo Kikuchi
Toru Miura
Takema Fukatsu
description Symbiosis often entails the emergence of novel adaptive traits in organisms. Microbial symbionts are indispensable for diverse insects via provisioning of essential nutrients, wherein novel host cells and organs for harboring the microbes, called bacteriocytes and bacteriomes, have evolved repeatedly. Molecular and developmental mechanisms underpinning the emergence of novel symbiotic cells and organs comprise an unsolved question in evolutionary developmental biology. Here, we report that a conserved homeotic gene, Ultrabithorax , plays a pivotal role in the bacteriocyte differentiation in a hemipteran insect Nysius plebeius . During embryonic development, six pairs of aggregated presumptive bacteriocytes appear on both sides of six abdominal segments, incorporate the symbiotic bacteria at the stage of germband retraction, and fuse into a pair of lateral bacteriomes at the stage of germband flip, where bacteriocyte-associated Ultrabithorax expression coincides with the symbiont infection process. Suppression of Ultrabithorax expression by maternal RNA interference results in disappearance of the bacteriocytes and the symbiont localization therein, suggesting that Ultrabithorax is involved in differentiation of the host cells for symbiosis. Suppression of other homeotic genes abdominal-A and Antennapedia disturbs integrity and positioning of the bacteriomes, affecting the configuration of the host organs for symbiosis. Our findings unveil the molecular and developmental mechanisms underlying the bacteriocyte differentiation, which may have evolved either via cooption of the transcription factors for inducing the novel symbiotic cells, or via revival of the developmental pathway for the bacteriocytes that had existed in the ancestral hemipterans. Among the most fundamental questions in developmental biology is how novel cell types have emerged in the metazoan evolution. Among the most challenging questions in evolutionary biology is how sophisticated symbiotic associations have evolved through less intimate interorganismal interactions. These fundamental biological issues are crystalized in the evolution and development of insect’s bacteriocytes specialized for harboring symbiotic bacteria. Here, we report that a conserved transcription factor Ultrabithorax is essential for bacteriocyte development in an insect, thereby uncovering a molecular mechanism underlying the emergence of the novel host cells for symbiosis. Our finding highlights the importance of
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Microbial symbionts are indispensable for diverse insects via provisioning of essential nutrients, wherein novel host cells and organs for harboring the microbes, called bacteriocytes and bacteriomes, have evolved repeatedly. Molecular and developmental mechanisms underpinning the emergence of novel symbiotic cells and organs comprise an unsolved question in evolutionary developmental biology. Here, we report that a conserved homeotic gene, Ultrabithorax , plays a pivotal role in the bacteriocyte differentiation in a hemipteran insect Nysius plebeius . During embryonic development, six pairs of aggregated presumptive bacteriocytes appear on both sides of six abdominal segments, incorporate the symbiotic bacteria at the stage of germband retraction, and fuse into a pair of lateral bacteriomes at the stage of germband flip, where bacteriocyte-associated Ultrabithorax expression coincides with the symbiont infection process. Suppression of Ultrabithorax expression by maternal RNA interference results in disappearance of the bacteriocytes and the symbiont localization therein, suggesting that Ultrabithorax is involved in differentiation of the host cells for symbiosis. Suppression of other homeotic genes abdominal-A and Antennapedia disturbs integrity and positioning of the bacteriomes, affecting the configuration of the host organs for symbiosis. Our findings unveil the molecular and developmental mechanisms underlying the bacteriocyte differentiation, which may have evolved either via cooption of the transcription factors for inducing the novel symbiotic cells, or via revival of the developmental pathway for the bacteriocytes that had existed in the ancestral hemipterans. Among the most fundamental questions in developmental biology is how novel cell types have emerged in the metazoan evolution. Among the most challenging questions in evolutionary biology is how sophisticated symbiotic associations have evolved through less intimate interorganismal interactions. These fundamental biological issues are crystalized in the evolution and development of insect’s bacteriocytes specialized for harboring symbiotic bacteria. Here, we report that a conserved transcription factor Ultrabithorax is essential for bacteriocyte development in an insect, thereby uncovering a molecular mechanism underlying the emergence of the novel host cells for symbiosis. 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Microbial symbionts are indispensable for diverse insects via provisioning of essential nutrients, wherein novel host cells and organs for harboring the microbes, called bacteriocytes and bacteriomes, have evolved repeatedly. Molecular and developmental mechanisms underpinning the emergence of novel symbiotic cells and organs comprise an unsolved question in evolutionary developmental biology. Here, we report that a conserved homeotic gene, Ultrabithorax , plays a pivotal role in the bacteriocyte differentiation in a hemipteran insect Nysius plebeius . During embryonic development, six pairs of aggregated presumptive bacteriocytes appear on both sides of six abdominal segments, incorporate the symbiotic bacteria at the stage of germband retraction, and fuse into a pair of lateral bacteriomes at the stage of germband flip, where bacteriocyte-associated Ultrabithorax expression coincides with the symbiont infection process. Suppression of Ultrabithorax expression by maternal RNA interference results in disappearance of the bacteriocytes and the symbiont localization therein, suggesting that Ultrabithorax is involved in differentiation of the host cells for symbiosis. Suppression of other homeotic genes abdominal-A and Antennapedia disturbs integrity and positioning of the bacteriomes, affecting the configuration of the host organs for symbiosis. Our findings unveil the molecular and developmental mechanisms underlying the bacteriocyte differentiation, which may have evolved either via cooption of the transcription factors for inducing the novel symbiotic cells, or via revival of the developmental pathway for the bacteriocytes that had existed in the ancestral hemipterans. Among the most fundamental questions in developmental biology is how novel cell types have emerged in the metazoan evolution. 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Microbial symbionts are indispensable for diverse insects via provisioning of essential nutrients, wherein novel host cells and organs for harboring the microbes, called bacteriocytes and bacteriomes, have evolved repeatedly. Molecular and developmental mechanisms underpinning the emergence of novel symbiotic cells and organs comprise an unsolved question in evolutionary developmental biology. Here, we report that a conserved homeotic gene, Ultrabithorax , plays a pivotal role in the bacteriocyte differentiation in a hemipteran insect Nysius plebeius . During embryonic development, six pairs of aggregated presumptive bacteriocytes appear on both sides of six abdominal segments, incorporate the symbiotic bacteria at the stage of germband retraction, and fuse into a pair of lateral bacteriomes at the stage of germband flip, where bacteriocyte-associated Ultrabithorax expression coincides with the symbiont infection process. Suppression of Ultrabithorax expression by maternal RNA interference results in disappearance of the bacteriocytes and the symbiont localization therein, suggesting that Ultrabithorax is involved in differentiation of the host cells for symbiosis. Suppression of other homeotic genes abdominal-A and Antennapedia disturbs integrity and positioning of the bacteriomes, affecting the configuration of the host organs for symbiosis. Our findings unveil the molecular and developmental mechanisms underlying the bacteriocyte differentiation, which may have evolved either via cooption of the transcription factors for inducing the novel symbiotic cells, or via revival of the developmental pathway for the bacteriocytes that had existed in the ancestral hemipterans. Among the most fundamental questions in developmental biology is how novel cell types have emerged in the metazoan evolution. 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source Jstor Complete Legacy; MEDLINE; Full-Text Journals in Chemistry (Open access); PubMed Central; Alma/SFX Local Collection
subjects Animalia
Animals
Bacteria
bacteriocyte
bacteriocytes
Base Sequence
Biological Sciences
Cells
Cloning, Molecular
Drosophila Proteins - physiology
evolution
Evolution, Molecular
Evolutionary biology
Female
Gene Expression Profiling
Gene Expression Regulation, Developmental
Genes
Hemiptera - microbiology
Hemiptera - physiology
Homeodomain Proteins - metabolism
Homeodomain Proteins - physiology
homeotic gene
In Situ Hybridization
insect development
Insect Proteins - physiology
Insects
Larva - microbiology
Larva - physiology
Male
Microscopy, Electron, Scanning
microsymbionts
Molecular Sequence Data
Nysius
Phenotype
Plebeius
RNA Interference
Symbiosis
transcription factor
transcription factors
Transcription Factors - metabolism
Transcription Factors - physiology
title Ultrabithorax is essential for bacteriocyte development
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