David Koller, Kevin M. Kocot, Bernard M. Degnan, Tim Wollesen
The eyes of squids, octopuses, and cuttlefish are a textbook example for evolutionary convergence, due to their striking similarity to those of vertebrates. For this reason, studies on cephalopod photoreception and vision are of importance for a broader audience. Previous studies showed that genes such as pax6, or certain opsin-encoding genes, are evolutionarily highly conserved and play similar roles during ontogenesis in remotely related bilaterians. In this study, genes that encode photosensitive proteins and Reflectins are identified and characterized. The expression patterns of rhodopsin, xenopsin, retinochrome, and two reflectin genes have been visualized in developing embryos of the pygmy squid Xipholeptos notoides by in situ hybridization experiments. Rhodopsin is not only expressed in the retina of X. notoides but also in the olfactory organ and the dorsal parolfactory vesicles, the latter a cephalopod apomorphy. Both reflectin genes are expressed in the eyes and in the olfactory organ. These findings corroborate previous studies that found opsin genes in the transcriptomes of the eyes and several extraocular tissues of various cephalopods. Expression of rhodopsin, xenopsin, retinochrome, and the two reflectin genes in the olfactory organ is a finding that has not been described so far. In other organisms, it has been shown that Retinochrome and Rhodopsin proteins are obligatorily associated with each other as both molecules rely on each other for Retinal isomerisation. In addition, we demonstrate that retinochrome is expressed in the retina of X. notoides and in the olfactory organ. This study shows numerous new expression patterns for Opsin-encoding genes in organs that have not been associated with photoreception before, suggesting that either Opsins may not only be involved in photoreception or organs such as the olfactory organ are involved in photoreception.
{"title":"Developmental gene expression in the eyes of the pygmy squid Xipholeptos notoides","authors":"David Koller, Kevin M. Kocot, Bernard M. Degnan, Tim Wollesen","doi":"10.1002/jez.b.23270","DOIUrl":"10.1002/jez.b.23270","url":null,"abstract":"<p>The eyes of squids, octopuses, and cuttlefish are a textbook example for evolutionary convergence, due to their striking similarity to those of vertebrates. For this reason, studies on cephalopod photoreception and vision are of importance for a broader audience. Previous studies showed that genes such as <i>pax6</i>, or certain opsin-encoding genes, are evolutionarily highly conserved and play similar roles during ontogenesis in remotely related bilaterians. In this study, genes that encode photosensitive proteins and Reflectins are identified and characterized. The expression patterns of <i>rhodopsin</i>, <i>xenopsin</i>, <i>retinochrome</i>, and two <i>reflectin</i> genes have been visualized in developing embryos of the pygmy squid <i>Xipholeptos notoides</i> by in situ hybridization experiments. <i>Rhodopsin</i> is not only expressed in the retina of <i>X. notoides</i> but also in the olfactory organ and the dorsal parolfactory vesicles, the latter a cephalopod apomorphy. Both <i>reflectin</i> genes are expressed in the eyes and in the olfactory organ. These findings corroborate previous studies that found <i>opsin</i> genes in the transcriptomes of the eyes and several extraocular tissues of various cephalopods. Expression of <i>rhodopsin</i>, <i>xenopsin</i>, <i>retinochrome</i>, and the two <i>reflectin</i> genes in the olfactory organ is a finding that has not been described so far. In other organisms, it has been shown that Retinochrome and Rhodopsin proteins are obligatorily associated with each other as both molecules rely on each other for Retinal isomerisation. In addition, we demonstrate that <i>retinochrome</i> is expressed in the retina of <i>X. notoides</i> and in the olfactory organ. This study shows numerous new expression patterns for Opsin-encoding genes in organs that have not been associated with photoreception before, suggesting that either Opsins may not only be involved in photoreception or organs such as the olfactory organ are involved in photoreception.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 7","pages":"483-498"},"PeriodicalIF":1.8,"publicationDate":"2024-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23270","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142004355","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tijana Vučić, Marija Drobnjaković, Maja Ajduković, Marko Bugarčić, Ben Wielstra, Ana Ivanović, Milena Cvijanović
There is an increased interest in the evolution and development of newts from the genus Triturus because: (1) morphological differentiation among the nine constituent species largely corresponds to different ecological preferences, (2) hybridization between different species pairs has various evolutionary outcomes in terms of life history traits and morphology, and (3) the genus expresses a balanced lethal system that causes arrested growth and death of half of the embryos. These features provide natural experimental settings for molecular, morphological, and life-history studies. Therefore, we produce a staging table for the Balkan crested newt (T. ivanbureschi). We provide detailed descriptions of 34 embryonic stages based on easily observable and interpretable external morphological characters, to ensure reproducibility. Compared with previous staging tables for Triturus, we include a vastly increased sample size and provide high-resolution photographs in lateral, ventral, and dorsal view, complemented by videos of specific developmental periods, and accompanied by detailed explanations on how to delineate the specific stages. Our staging table will serve as a baseline in comparative studies on Triturus newts: an emerging model system in evolutionary and developmental studies.
{"title":"A staging table of Balkan crested newt embryonic development to serve as a baseline in evolutionary developmental studies","authors":"Tijana Vučić, Marija Drobnjaković, Maja Ajduković, Marko Bugarčić, Ben Wielstra, Ana Ivanović, Milena Cvijanović","doi":"10.1002/jez.b.23269","DOIUrl":"10.1002/jez.b.23269","url":null,"abstract":"<p>There is an increased interest in the evolution and development of newts from the genus <i>Triturus</i> because: (1) morphological differentiation among the nine constituent species largely corresponds to different ecological preferences, (2) hybridization between different species pairs has various evolutionary outcomes in terms of life history traits and morphology, and (3) the genus expresses a balanced lethal system that causes arrested growth and death of half of the embryos. These features provide natural experimental settings for molecular, morphological, and life-history studies. Therefore, we produce a staging table for the Balkan crested newt (<i>T. ivanbureschi</i>). We provide detailed descriptions of 34 embryonic stages based on easily observable and interpretable external morphological characters, to ensure reproducibility. Compared with previous staging tables for <i>Triturus</i>, we include a vastly increased sample size and provide high-resolution photographs in lateral, ventral, and dorsal view, complemented by videos of specific developmental periods, and accompanied by detailed explanations on how to delineate the specific stages. Our staging table will serve as a baseline in comparative studies on <i>Triturus</i> newts: an emerging model system in evolutionary and developmental studies.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 7","pages":"465-482"},"PeriodicalIF":1.8,"publicationDate":"2024-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23269","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141476677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mai P. Tran, Daniel Ochoa Reyes, Alexander J. Weitzel, Aditya Saxena, Michael Hiller, Kimberly L. Cooper
Vertebrate animals that run or jump across sparsely vegetated habitats, such as horses and jerboas, have reduced the number of distal limb bones, and many have lost most or all distal limb muscle. We previously showed that nascent muscles are present in the jerboa hindfoot at birth and that these myofibers are rapidly and completely lost soon after by a process that shares features with pathological skeletal muscle atrophy. Here, we apply an intra- and interspecies differential RNA-Seq approach, comparing jerboa and mouse muscles, to identify gene expression differences associated with the initiation and progression of jerboa hindfoot muscle loss. We show evidence for reduced hepatocyte growth factor and fibroblast growth factor signaling and an imbalance in nitric oxide signaling; all are pathways that are necessary for skeletal muscle development and regeneration. We also find evidence for phagosome formation, which hints at how myofibers may be removed by autophagy or by nonprofessional phagocytes without evidence for cell death or immune cell activation. Last, we show significant overlap between genes associated with jerboa hindfoot muscle loss and genes that are differentially expressed in a variety of human muscle pathologies and rodent models of muscle loss disorders. All together, these data provide molecular insight into the process of evolutionary and developmental muscle loss in jerboa hindfeet.
{"title":"Gene expression differences associated with intrinsic hindfoot muscle loss in the jerboa, Jaculus jaculus","authors":"Mai P. Tran, Daniel Ochoa Reyes, Alexander J. Weitzel, Aditya Saxena, Michael Hiller, Kimberly L. Cooper","doi":"10.1002/jez.b.23268","DOIUrl":"10.1002/jez.b.23268","url":null,"abstract":"<p>Vertebrate animals that run or jump across sparsely vegetated habitats, such as horses and jerboas, have reduced the number of distal limb bones, and many have lost most or all distal limb muscle. We previously showed that nascent muscles are present in the jerboa hindfoot at birth and that these myofibers are rapidly and completely lost soon after by a process that shares features with pathological skeletal muscle atrophy. Here, we apply an intra- and interspecies differential RNA-Seq approach, comparing jerboa and mouse muscles, to identify gene expression differences associated with the initiation and progression of jerboa hindfoot muscle loss. We show evidence for reduced hepatocyte growth factor and fibroblast growth factor signaling and an imbalance in nitric oxide signaling; all are pathways that are necessary for skeletal muscle development and regeneration. We also find evidence for phagosome formation, which hints at how myofibers may be removed by autophagy or by nonprofessional phagocytes without evidence for cell death or immune cell activation. Last, we show significant overlap between genes associated with jerboa hindfoot muscle loss and genes that are differentially expressed in a variety of human muscle pathologies and rodent models of muscle loss disorders. All together, these data provide molecular insight into the process of evolutionary and developmental muscle loss in jerboa hindfeet.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 7","pages":"453-464"},"PeriodicalIF":1.8,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23268","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141468502","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Guillaume Poncelet, Lucia Parolini, Sebastian M. Shimeld
Sea squirts (Tunicata) are chordates and develop a swimming larva with a small and defined number of individually identifiable cells. This offers the prospect of connecting specific stimuli to behavioral output and characterizing the neural activity that links these together. Here, we describe the development of a microfluidic chip that allows live larvae of the sea squirt Ciona intestinalis to be immobilized and recorded. By generating transgenic larvae expressing GCaAMP6m in defined cells, we show that calcium ion levels can be recorded from immobilized larvae, while microfluidic control allows larvae to be exposed to specific waterborne stimuli. We trial this on sea water carrying increased levels of carbon dioxide, providing evidence that larvae can sense this gas.
{"title":"A microfluidic chip for immobilization and imaging of Ciona intestinalis larvae","authors":"Guillaume Poncelet, Lucia Parolini, Sebastian M. Shimeld","doi":"10.1002/jez.b.23267","DOIUrl":"10.1002/jez.b.23267","url":null,"abstract":"<p>Sea squirts (Tunicata) are chordates and develop a swimming larva with a small and defined number of individually identifiable cells. This offers the prospect of connecting specific stimuli to behavioral output and characterizing the neural activity that links these together. Here, we describe the development of a microfluidic chip that allows live larvae of the sea squirt <i>Ciona intestinalis</i> to be immobilized and recorded. By generating transgenic larvae expressing GCaAMP6m in defined cells, we show that calcium ion levels can be recorded from immobilized larvae, while microfluidic control allows larvae to be exposed to specific waterborne stimuli. We trial this on sea water carrying increased levels of carbon dioxide, providing evidence that larvae can sense this gas.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 7","pages":"443-452"},"PeriodicalIF":1.8,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23267","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141283805","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Žiga Fišer, Hana Whitehorn, Tia Furness, Peter Trontelj, Meredith Protas
Similar phenotypes can evolve repeatedly under the same evolutionary pressures. A compelling example is the evolution of pigment loss and eye loss in cave-dwelling animals. While specific genomic regions or genes associated with these phenotypes have been identified in model species, it remains uncertain whether a bias towards particular genetic mechanisms exists. An isopod crustacean, Asellus aquaticus, is an ideal model organism to investigate this phenomenon. It inhabits surface freshwaters throughout Europe but has colonized groundwater on multiple independent occasions and evolved several cave populations with distinct ecomorphology. Previous studies have demonstrated that three different cave populations utilized common genetic regions, potentially the same genes, in the evolution of pigment and eye loss. Expanding on this, we conducted analysis on two additional cave populations, distinct either phylogenetically or biogeographically from those previously examined. We generated F2 hybrids from cave × surface crosses and tested phenotype-genotype associations, as well as conducted complementation tests by crossing individuals from different cave populations. Our findings revealed that pigment loss and orange eye pigment in additional cave populations were associated with the same genomic regions as observed in the three previously tested cave populations. Moreover, the lack of complementation across all cross combinations suggests that the same gene likely drives pigment loss. These results substantiate a genetic bias in the recurrent evolution of pigment loss in this model system. Future investigations should focus on the cause behind this bias, possibly arising from allele recruitment from ancestral surface populations' genetic variation or advantageous allele effects via pleiotropy.
{"title":"Genetic bias in repeated evolution of pigment loss in cave populations of the Asellus aquaticus species complex","authors":"Žiga Fišer, Hana Whitehorn, Tia Furness, Peter Trontelj, Meredith Protas","doi":"10.1002/jez.b.23256","DOIUrl":"10.1002/jez.b.23256","url":null,"abstract":"<p>Similar phenotypes can evolve repeatedly under the same evolutionary pressures. A compelling example is the evolution of pigment loss and eye loss in cave-dwelling animals. While specific genomic regions or genes associated with these phenotypes have been identified in model species, it remains uncertain whether a bias towards particular genetic mechanisms exists. An isopod crustacean, <i>Asellus aquaticus</i>, is an ideal model organism to investigate this phenomenon. It inhabits surface freshwaters throughout Europe but has colonized groundwater on multiple independent occasions and evolved several cave populations with distinct ecomorphology. Previous studies have demonstrated that three different cave populations utilized common genetic regions, potentially the same genes, in the evolution of pigment and eye loss. Expanding on this, we conducted analysis on two additional cave populations, distinct either phylogenetically or biogeographically from those previously examined. We generated F2 hybrids from cave × surface crosses and tested phenotype-genotype associations, as well as conducted complementation tests by crossing individuals from different cave populations. Our findings revealed that pigment loss and orange eye pigment in additional cave populations were associated with the same genomic regions as observed in the three previously tested cave populations. Moreover, the lack of complementation across all cross combinations suggests that the same gene likely drives pigment loss. These results substantiate a genetic bias in the recurrent evolution of pigment loss in this model system. Future investigations should focus on the cause behind this bias, possibly arising from allele recruitment from ancestral surface populations' genetic variation or advantageous allele effects via pleiotropy.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 6","pages":"425-436"},"PeriodicalIF":1.8,"publicationDate":"2024-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23256","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141198917","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"In the Spotlight—Established researcher","authors":"Janine M. Ziermann-Canabarro","doi":"10.1002/jez.b.23257","DOIUrl":"10.1002/jez.b.23257","url":null,"abstract":"","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 6","pages":"417-418"},"PeriodicalIF":1.8,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141081680","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"In the Spotlight: Established researcher","authors":"Virginia Abdala","doi":"10.1002/jez.b.23258","DOIUrl":"10.1002/jez.b.23258","url":null,"abstract":"","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 5","pages":"389-390"},"PeriodicalIF":2.2,"publicationDate":"2024-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141065725","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Astrid K. Lisondro-Arosemena, María José Salazar-Nicholls, Karen M. Warkentin
Egg dehydration can kill terrestrial frog embryos, and this threat is increasing with climate change and deforestation. In several lineages that independently evolved terrestrial eggs, and retained aquatic tadpoles, embryos accelerate hatching to escape from drying eggs, entering the water earlier and less developed. However, the cues that stimulate drying-induced early hatching are unknown. Ammonia is a toxic, water-soluble metabolic waste that accumulates within eggs as embryos develop and concentrates as eggs dehydrate. Thus, increasing ammonia concentration may be a direct threat to embryos in drying eggs. We hypothesized that it could serve as a cue, stimulating embryos to hatch and escape. The embryos of red-eyed treefrogs, Agalychnis callidryas, hatch early to escape from many threats, including dehydration, and are known to use mechanosensory, hypoxia, and light cues. To test if they also use high ammonia as a cue to hatch, we exposed stage-matched pairs of hatching-competent, well-hydrated sibling embryos to ammonia and control solutions in shallow water baths and recorded their behavior. Control embryos remained unhatched while ammonia-exposed embryos showed a rapid, strong hatching response; 95% hatched, on average in under 15 min. This demonstrates that elevated ammonia can serve as a hatching cue for A. callidryas embryos. This finding is a key step in understanding the mechanisms that enable terrestrial frog embryos to escape from egg drying, opening new possibilities for integrative and comparative studies on this growing threat.
{"title":"Elevated ammonia cues hatching in red-eyed treefrogs: A mechanism for escape from drying eggs","authors":"Astrid K. Lisondro-Arosemena, María José Salazar-Nicholls, Karen M. Warkentin","doi":"10.1002/jez.b.23253","DOIUrl":"10.1002/jez.b.23253","url":null,"abstract":"<p>Egg dehydration can kill terrestrial frog embryos, and this threat is increasing with climate change and deforestation. In several lineages that independently evolved terrestrial eggs, and retained aquatic tadpoles, embryos accelerate hatching to escape from drying eggs, entering the water earlier and less developed. However, the cues that stimulate drying-induced early hatching are unknown. Ammonia is a toxic, water-soluble metabolic waste that accumulates within eggs as embryos develop and concentrates as eggs dehydrate. Thus, increasing ammonia concentration may be a direct threat to embryos in drying eggs. We hypothesized that it could serve as a cue, stimulating embryos to hatch and escape. The embryos of red-eyed treefrogs, <i>Agalychnis callidryas</i>, hatch early to escape from many threats, including dehydration, and are known to use mechanosensory, hypoxia, and light cues. To test if they also use high ammonia as a cue to hatch, we exposed stage-matched pairs of hatching-competent, well-hydrated sibling embryos to ammonia and control solutions in shallow water baths and recorded their behavior. Control embryos remained unhatched while ammonia-exposed embryos showed a rapid, strong hatching response; 95% hatched, on average in under 15 min. This demonstrates that elevated ammonia can serve as a hatching cue for <i>A. callidryas</i> embryos. This finding is a key step in understanding the mechanisms that enable terrestrial frog embryos to escape from egg drying, opening new possibilities for integrative and comparative studies on this growing threat.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 5","pages":"406-411"},"PeriodicalIF":2.2,"publicationDate":"2024-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140851108","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
<p></p><p>Ingo is a Guest Coeditor of this special issue on <i>Aquatic Models for Biomedical Evo-Devo</i>.</p><p>Website: https://www.fishevodevogeno.org/</p><p>Google scholar page: https://scholar.google.com/citations?user=xVw8dCAAAAAJ</p><p>I studied biology at the University of Konstanz, Germany, and worked as an undergraduate on my first comparative fish genomics projects in the group of Axel Meyer with two fantastic postdocs at the time: John S. Taylor, now faculty at the University of Victoria, Canada, and Walter Salzburger, now faculty at the University of Basel, Switzerland. For my doctoral work, I joined Manfred Schartl and Jean-Nicolas Volff at the University of Würzburg, also in Germany, studying the functional genetic impacts of whole genome duplications on the evolution of vertebrate pigmentation. For my postdoc, I worked in the group of John H. Postlethwait at the University of Oregon in Eugene. John's group had just started to use spotted gar as a genomic outgroup to the teleost fishes and the teleost genome duplication. There, I began developing spotted gar as a developmental and functional genomic model system for vertebrate biology and EvoDevo – work that continues in my laboratory at Michigan State University.</p><p>I grew up in provincial Germany as the son of a high school chemistry and physics teacher and a pharmaceutical technician, so I was exposed to the natural sciences early on. Starting in elementary school, I developed a passion for reading about dinosaurs and prehistoric people, years before <i>Jurassic Park</i> made paleontology cool. Thus, although I didn't know the term then, I had an early appreciation for macroevolution. In high school, I kept all kinds of aquarium fishes (can you ever have too many tanks?), while reading about Darwin's <i>Voyage of the Beagle</i>, evolution, and genetics. This fascination kept going and was a reason I chose the University of Konstanz for undergraduate studies because of its strong curricular focus on molecular biology. Working as an undergraduate researcher in the Meyer Lab and being surrounded by an international crew of world-class molecular evolutionary biologists around me – who even used fish models to answer big questions about the deep evolutionary history of vertebrates – was immensely thrilling. Comparing sequences from diverse organisms and reconstructing their evolutionary change across phylogenies, I could practically look back in time! I knew I had found my path. However, sequencing DNA and analyzing genetic information on the computer was not enough for me. Fondly remembering my childhood fish breeding projects and the beauty of watching fish embryos grow, I successively added developmental biology to my research portfolio. The name of my research group, the <i>Fish Evo Devo Geno Lab</i>, reflects this multipronged approach.</p><p>Observing the elegance of developmental processes in many different fish species is my happy place. How could anyone ever just want to
Ingo是本期 "生物医学进化论的水生模型 "特刊的客座联合编辑。网站:https://www.fishevodevogeno.org/Google 学术网页:https://scholar.google.com/citations?user=xVw8dCAAAAAJI 在德国康斯坦茨大学攻读生物学,本科时曾在阿克塞尔-迈耶(Axel Meyer)的小组与当时两位出色的博士后一起从事我的第一个比较鱼类基因组学项目:约翰-泰勒(John S. Taylor,现任加拿大维多利亚大学教师)和沃尔特-萨尔茨伯格(Walter Salzburger,现任瑞士巴塞尔大学教师)。博士期间,我加入了德国维尔茨堡大学的曼弗雷德-沙特尔(Manfred Schartl)和让-尼古拉斯-沃尔夫(Jean-Nicolas Volff)的团队,研究全基因组复制对脊椎动物色素进化的功能性遗传影响。博士后期间,我在尤金俄勒冈大学约翰-H-波斯特斯韦特(John H. Postlethwait)小组工作。当时约翰的研究小组刚刚开始将斑鲤作为长尾鱼类和长尾鱼类基因组复制的基因组外群。在那里,我开始将斑点叉尾鮰作为脊椎动物生物学和进化论的发育和功能基因组模型系统进行开发,我在密歇根州立大学的实验室继续这项工作。我在德国外省长大,父亲是中学化学和物理教师,母亲是制药技师,因此我很早就接触到自然科学。从小学开始,我就热衷于阅读有关恐龙和史前人类的书籍,这比《侏罗纪公园》让古生物学变酷还要早几年。因此,虽然当时我还不知道这个词,但我很早就对宏观进化有了认识。高中时,我饲养了各种各样的鱼类(鱼缸再多也不为过),同时阅读了达尔文的《小猎犬号航行记》、进化论和遗传学方面的书籍。这种痴迷一直持续到现在,这也是我选择康斯坦茨大学攻读本科的原因之一,因为该校的分子生物学课程重点突出。在迈耶实验室担任本科生研究员,身边围绕着一群世界一流的分子进化生物学家--他们甚至用鱼类模型来解答脊椎动物深层进化史的重大问题--让我感到无比兴奋。比较来自不同生物的序列,重建它们在不同系统发育过程中的进化变化,我几乎可以回望过去!我知道自己找到了方向。然而,DNA测序和在电脑上分析遗传信息对我来说还远远不够。回想起儿时的养鱼计划和观察鱼胚胎成长的美好时光,我陆续将发育生物学加入了我的研究领域。我的研究小组名为 "鱼类进化发育基因实验室"(Fish Evo Devo Geno Lab),反映了这种多管齐下的研究方法。怎么会有人只想研究一种生物呢?在我的研究生涯中,我研究过斑马鱼、青鳉、慈鲷、鸭嘴鱼和剑尾鱼、鳉鱼、嘎尔鱼、弓鳍鱼等等,更不用说我们还分析了所有的鱼类基因组。在我看来,这正是进化胚胎学研究的核心所在--能够欣赏、研究,有时甚至解开 "无穷无尽的最美形态 "的一些机制基础。与此同时,由于没有一个实验室能保留所有的模式生物,也没有一个实验室能成为所有必要方法的专家,因此比较进化胚胎学研究本质上是合作性的,而且我强烈认为,它还特别具有开放性思维和开阔性思维。随着基因组学、基因组编辑、转基因、体内成像以及包括人工智能在内的计算技术的惊人进步,我们显然将迎来一个伟大的时代。大量的相关数据需要在不同的研究生物体中进行功能测试,以便在基因型和表型之间建立实际的因果联系--自然,EvoDevo 研究将引领这一潮流。由于我们这个领域的跨学科性质,您可能会发现自己经常处于这样的境地--无论是在研究生院、在会议上,还是在您新加入的系里--您的思维方式、想法和研究被认为超出了我们旨在整合的任何专业学科的主流。让您的 EvoDevo 研究既能吸引基础研究,也能吸引更多的应用和生物医学资助机制。保持自信,胸怀大局,相信自己有能力超越个别研究领域的知识孤岛和障眼法。幸运的是,随着泛美进化发育生物学学会和欧洲进化发育生物学学会在过去20年中的成立,我个人认为这是我的知识家园,我们现在有很多机会在我们热闹的社区中建立联系,共同倡导EvoDevo思想。快来加入我们吧
{"title":"In the Spotlight—Established researcher","authors":"Ingo Braasch","doi":"10.1002/jez.b.23254","DOIUrl":"https://doi.org/10.1002/jez.b.23254","url":null,"abstract":"<p></p><p>Ingo is a Guest Coeditor of this special issue on <i>Aquatic Models for Biomedical Evo-Devo</i>.</p><p>Website: https://www.fishevodevogeno.org/</p><p>Google scholar page: https://scholar.google.com/citations?user=xVw8dCAAAAAJ</p><p>I studied biology at the University of Konstanz, Germany, and worked as an undergraduate on my first comparative fish genomics projects in the group of Axel Meyer with two fantastic postdocs at the time: John S. Taylor, now faculty at the University of Victoria, Canada, and Walter Salzburger, now faculty at the University of Basel, Switzerland. For my doctoral work, I joined Manfred Schartl and Jean-Nicolas Volff at the University of Würzburg, also in Germany, studying the functional genetic impacts of whole genome duplications on the evolution of vertebrate pigmentation. For my postdoc, I worked in the group of John H. Postlethwait at the University of Oregon in Eugene. John's group had just started to use spotted gar as a genomic outgroup to the teleost fishes and the teleost genome duplication. There, I began developing spotted gar as a developmental and functional genomic model system for vertebrate biology and EvoDevo – work that continues in my laboratory at Michigan State University.</p><p>I grew up in provincial Germany as the son of a high school chemistry and physics teacher and a pharmaceutical technician, so I was exposed to the natural sciences early on. Starting in elementary school, I developed a passion for reading about dinosaurs and prehistoric people, years before <i>Jurassic Park</i> made paleontology cool. Thus, although I didn't know the term then, I had an early appreciation for macroevolution. In high school, I kept all kinds of aquarium fishes (can you ever have too many tanks?), while reading about Darwin's <i>Voyage of the Beagle</i>, evolution, and genetics. This fascination kept going and was a reason I chose the University of Konstanz for undergraduate studies because of its strong curricular focus on molecular biology. Working as an undergraduate researcher in the Meyer Lab and being surrounded by an international crew of world-class molecular evolutionary biologists around me – who even used fish models to answer big questions about the deep evolutionary history of vertebrates – was immensely thrilling. Comparing sequences from diverse organisms and reconstructing their evolutionary change across phylogenies, I could practically look back in time! I knew I had found my path. However, sequencing DNA and analyzing genetic information on the computer was not enough for me. Fondly remembering my childhood fish breeding projects and the beauty of watching fish embryos grow, I successively added developmental biology to my research portfolio. The name of my research group, the <i>Fish Evo Devo Geno Lab</i>, reflects this multipronged approach.</p><p>Observing the elegance of developmental processes in many different fish species is my happy place. How could anyone ever just want to ","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 3","pages":"121-122"},"PeriodicalIF":2.2,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23254","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140814166","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Patricia N. Schneider, Frauke Seemann, Matthew P. Harris, Ingo Braasch
{"title":"Trawling aquatic life for new models in biomedical research and evolutionary developmental biology","authors":"Patricia N. Schneider, Frauke Seemann, Matthew P. Harris, Ingo Braasch","doi":"10.1002/jez.b.23255","DOIUrl":"https://doi.org/10.1002/jez.b.23255","url":null,"abstract":"","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 3","pages":"123-125"},"PeriodicalIF":2.2,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23255","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140814167","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}