José Luis Juárez-Morales, Frida Weierud, Samantha J. England, Celia Demby, Nicole Santos, Ginny Grieb, Sylvie Mazan, Katharine E. Lewis
{"title":"lbx脊髓表达和功能的进化。","authors":"José Luis Juárez-Morales, Frida Weierud, Samantha J. England, Celia Demby, Nicole Santos, Ginny Grieb, Sylvie Mazan, Katharine E. Lewis","doi":"10.1111/ede.12387","DOIUrl":null,"url":null,"abstract":"<p>Ladybird homeobox (Lbx) transcription factors have crucial functions in muscle and nervous system development in many animals. Amniotes have two <i>Lbx</i> genes, but only <i>Lbx1</i> is expressed in spinal cord. In contrast, teleosts have three <i>lbx</i> genes and we show here that zebrafish <i>lbx1a</i>, <i>lbx1b</i>, and <i>lbx2</i> are expressed by distinct spinal cell types, and that <i>lbx1a</i> is expressed in dI4, dI5, and dI6 interneurons, as in amniotes. Our data examining <i>lbx</i> expression in <i>Scyliorhinus canicula</i> and <i>Xenopus tropicalis</i> suggest that the spinal interneuron expression of zebrafish <i>lbx1a</i> is ancestral, whereas <i>lbx1b</i> has acquired a new expression pattern in spinal cord progenitor cells. <i>lbx2</i> spinal expression was probably acquired in the ray-finned lineage, as this gene is not expressed in the spinal cords of either amniotes or <i>S. canicula</i>. We also show that the spinal function of zebrafish <i>lbx1a</i> is conserved with mouse Lbx1. In zebrafish <i>lbx1a</i> mutants, there is a reduction in the number of inhibitory spinal interneurons and an increase in the number of excitatory spinal interneurons, similar to mouse <i>Lbx1</i> mutants. Interestingly, the number of inhibitory spinal interneurons is also reduced in <i>lbx1b</i> mutants, although in this case the number of excitatory interneurons is not increased. <i>lbx1a;lbx1b</i> double mutants have a similar spinal interneuron phenotype to <i>lbx1a</i> single mutants. Taken together these data suggest that <i>lbx1b</i> and <i>lbx1a</i> may be required in succession for correct specification of dI4 and dI6 spinal interneurons, although only <i>lbx1a</i> is required for suppression of excitatory fates in these cells.</p>","PeriodicalId":12083,"journal":{"name":"Evolution & Development","volume":"23 5","pages":"404-422"},"PeriodicalIF":2.6000,"publicationDate":"2021-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/ede.12387","citationCount":"4","resultStr":"{\"title\":\"Evolution of lbx spinal cord expression and function\",\"authors\":\"José Luis Juárez-Morales, Frida Weierud, Samantha J. England, Celia Demby, Nicole Santos, Ginny Grieb, Sylvie Mazan, Katharine E. Lewis\",\"doi\":\"10.1111/ede.12387\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Ladybird homeobox (Lbx) transcription factors have crucial functions in muscle and nervous system development in many animals. Amniotes have two <i>Lbx</i> genes, but only <i>Lbx1</i> is expressed in spinal cord. In contrast, teleosts have three <i>lbx</i> genes and we show here that zebrafish <i>lbx1a</i>, <i>lbx1b</i>, and <i>lbx2</i> are expressed by distinct spinal cell types, and that <i>lbx1a</i> is expressed in dI4, dI5, and dI6 interneurons, as in amniotes. Our data examining <i>lbx</i> expression in <i>Scyliorhinus canicula</i> and <i>Xenopus tropicalis</i> suggest that the spinal interneuron expression of zebrafish <i>lbx1a</i> is ancestral, whereas <i>lbx1b</i> has acquired a new expression pattern in spinal cord progenitor cells. <i>lbx2</i> spinal expression was probably acquired in the ray-finned lineage, as this gene is not expressed in the spinal cords of either amniotes or <i>S. canicula</i>. We also show that the spinal function of zebrafish <i>lbx1a</i> is conserved with mouse Lbx1. In zebrafish <i>lbx1a</i> mutants, there is a reduction in the number of inhibitory spinal interneurons and an increase in the number of excitatory spinal interneurons, similar to mouse <i>Lbx1</i> mutants. Interestingly, the number of inhibitory spinal interneurons is also reduced in <i>lbx1b</i> mutants, although in this case the number of excitatory interneurons is not increased. <i>lbx1a;lbx1b</i> double mutants have a similar spinal interneuron phenotype to <i>lbx1a</i> single mutants. Taken together these data suggest that <i>lbx1b</i> and <i>lbx1a</i> may be required in succession for correct specification of dI4 and dI6 spinal interneurons, although only <i>lbx1a</i> is required for suppression of excitatory fates in these cells.</p>\",\"PeriodicalId\":12083,\"journal\":{\"name\":\"Evolution & Development\",\"volume\":\"23 5\",\"pages\":\"404-422\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2021-08-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1111/ede.12387\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Evolution & Development\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/ede.12387\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"DEVELOPMENTAL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolution & Development","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ede.12387","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
Evolution of lbx spinal cord expression and function
Ladybird homeobox (Lbx) transcription factors have crucial functions in muscle and nervous system development in many animals. Amniotes have two Lbx genes, but only Lbx1 is expressed in spinal cord. In contrast, teleosts have three lbx genes and we show here that zebrafish lbx1a, lbx1b, and lbx2 are expressed by distinct spinal cell types, and that lbx1a is expressed in dI4, dI5, and dI6 interneurons, as in amniotes. Our data examining lbx expression in Scyliorhinus canicula and Xenopus tropicalis suggest that the spinal interneuron expression of zebrafish lbx1a is ancestral, whereas lbx1b has acquired a new expression pattern in spinal cord progenitor cells. lbx2 spinal expression was probably acquired in the ray-finned lineage, as this gene is not expressed in the spinal cords of either amniotes or S. canicula. We also show that the spinal function of zebrafish lbx1a is conserved with mouse Lbx1. In zebrafish lbx1a mutants, there is a reduction in the number of inhibitory spinal interneurons and an increase in the number of excitatory spinal interneurons, similar to mouse Lbx1 mutants. Interestingly, the number of inhibitory spinal interneurons is also reduced in lbx1b mutants, although in this case the number of excitatory interneurons is not increased. lbx1a;lbx1b double mutants have a similar spinal interneuron phenotype to lbx1a single mutants. Taken together these data suggest that lbx1b and lbx1a may be required in succession for correct specification of dI4 and dI6 spinal interneurons, although only lbx1a is required for suppression of excitatory fates in these cells.
期刊介绍:
Evolution & Development serves as a voice for the rapidly growing research community at the interface of evolutionary and developmental biology. The exciting re-integration of these two fields, after almost a century''s separation, holds much promise as the focus of a broader synthesis of biological thought. Evolution & Development publishes works that address the evolution/development interface from a diversity of angles. The journal welcomes papers from paleontologists, population biologists, developmental biologists, and molecular biologists, but also encourages submissions from professionals in other fields where relevant research is being carried out, from mathematics to the history and philosophy of science.