Emma Johnson, Talbot Kinney, Hannah Luellen, Rhiannan Amerud, Daysha R Anderson, Marie Anderson, Arnelyn Mae Andres, Rameel Arshad, Kylie Babin-Howard, Dede G Barrigah, Addison Beauregard, Leah Beise, Nolan Christofferson, Elijah L David, Luke DeWaard, Maya Diaz, Lily Donner, Natalie Ehlinger, Diellza Elmazi, Riley Engelhardt, Tamkanat Farheen, Mark M Figueroa, Soren Flaten, Madison Frush, Elizabeth Gonzalez, Jaylen Goolsby, Estefania Guzman, Logan Hanson, John Hejl, Jackson Heuschel, Brianna Higgins, Brylee Hoeppner, Daijah Hollins, Josette Knutson, Rachel Lemont, Mia Lopez, Samantha Martin, Trinity May, Abby McDade, Nearyroth Men, Ellie Meyer, Caroline R Mickle, Sebastian Mireles, Avery Mize, Jaiden Neuhaus, April Ost, Sarah Piane, Makenzie Pianovski, Aliya Rangel, Jessica Reyes, Alexandra Ruttenberg, Jacob D Sachs, Brandon Schluns, Nicholas Schroeder, Peighton R Skrobot, Cylie Smith, Sydney Stout, Andrew Valenzuela, Kaiden P Vinavich, Amber K Weaver, Michael Yager, Jose Zaragoza, Gabriela Zawadzki, Weam El Rahmany, Nicole L Scheuermann, Hemin P Shah, Kayla L Bieser, Paula Croonquist, Olivier Devergne, Elizabeth E Taylor, Jacqueline K Wittke-Thompson, Jacob D Kagey, Stephanie Toering Peters
{"title":"E.3.3--一种新的致命等位基因的遗传图谱","authors":"Emma Johnson, Talbot Kinney, Hannah Luellen, Rhiannan Amerud, Daysha R Anderson, Marie Anderson, Arnelyn Mae Andres, Rameel Arshad, Kylie Babin-Howard, Dede G Barrigah, Addison Beauregard, Leah Beise, Nolan Christofferson, Elijah L David, Luke DeWaard, Maya Diaz, Lily Donner, Natalie Ehlinger, Diellza Elmazi, Riley Engelhardt, Tamkanat Farheen, Mark M Figueroa, Soren Flaten, Madison Frush, Elizabeth Gonzalez, Jaylen Goolsby, Estefania Guzman, Logan Hanson, John Hejl, Jackson Heuschel, Brianna Higgins, Brylee Hoeppner, Daijah Hollins, Josette Knutson, Rachel Lemont, Mia Lopez, Samantha Martin, Trinity May, Abby McDade, Nearyroth Men, Ellie Meyer, Caroline R Mickle, Sebastian Mireles, Avery Mize, Jaiden Neuhaus, April Ost, Sarah Piane, Makenzie Pianovski, Aliya Rangel, Jessica Reyes, Alexandra Ruttenberg, Jacob D Sachs, Brandon Schluns, Nicholas Schroeder, Peighton R Skrobot, Cylie Smith, Sydney Stout, Andrew Valenzuela, Kaiden P Vinavich, Amber K Weaver, Michael Yager, Jose Zaragoza, Gabriela Zawadzki, Weam El Rahmany, Nicole L Scheuermann, Hemin P Shah, Kayla L Bieser, Paula Croonquist, Olivier Devergne, Elizabeth E Taylor, Jacqueline K Wittke-Thompson, Jacob D Kagey, Stephanie Toering Peters","doi":"10.17912/micropub.biology.001236","DOIUrl":null,"url":null,"abstract":"<p><p>The <i>E.3.3</i> mutation was generated in a Flp/FRT EMS screen for conditional mutations that cause growth and developmental defects in a genetic background that blocks apoptosis. The mutations were conditional, based on the <i>Dark <sup>82</sup></i> allele being present on the starting chromosome, and blocking canonical apoptosis in a homozygous state. The <i>E.3.3</i> mosaic eyes exhibit defects in eye development including patches of rough eye and irregular surface structure. Whole Genome Sequencing and complementation mapping revealed <i>E.3.3</i> as an allele of <i>prod</i> . Prod is a DNA-binding protein that binds satellite repeats and is involved in chromocenter formation during mitosis. Here we present a novel allele of <i>prod</i> , <i>prod <sup>E.3.3</sup></i> , that disrupts the functional region of the Prod protein resulting in disruption of typical eye structure, likely due to disruption of chromatid separation during development.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11320118/pdf/","citationCount":"0","resultStr":"{\"title\":\"Genetic Mapping of <i>prod <sup>E.3.3</sup></i> , a New Lethal Allele of <i>prod</i>.\",\"authors\":\"Emma Johnson, Talbot Kinney, Hannah Luellen, Rhiannan Amerud, Daysha R Anderson, Marie Anderson, Arnelyn Mae Andres, Rameel Arshad, Kylie Babin-Howard, Dede G Barrigah, Addison Beauregard, Leah Beise, Nolan Christofferson, Elijah L David, Luke DeWaard, Maya Diaz, Lily Donner, Natalie Ehlinger, Diellza Elmazi, Riley Engelhardt, Tamkanat Farheen, Mark M Figueroa, Soren Flaten, Madison Frush, Elizabeth Gonzalez, Jaylen Goolsby, Estefania Guzman, Logan Hanson, John Hejl, Jackson Heuschel, Brianna Higgins, Brylee Hoeppner, Daijah Hollins, Josette Knutson, Rachel Lemont, Mia Lopez, Samantha Martin, Trinity May, Abby McDade, Nearyroth Men, Ellie Meyer, Caroline R Mickle, Sebastian Mireles, Avery Mize, Jaiden Neuhaus, April Ost, Sarah Piane, Makenzie Pianovski, Aliya Rangel, Jessica Reyes, Alexandra Ruttenberg, Jacob D Sachs, Brandon Schluns, Nicholas Schroeder, Peighton R Skrobot, Cylie Smith, Sydney Stout, Andrew Valenzuela, Kaiden P Vinavich, Amber K Weaver, Michael Yager, Jose Zaragoza, Gabriela Zawadzki, Weam El Rahmany, Nicole L Scheuermann, Hemin P Shah, Kayla L Bieser, Paula Croonquist, Olivier Devergne, Elizabeth E Taylor, Jacqueline K Wittke-Thompson, Jacob D Kagey, Stephanie Toering Peters\",\"doi\":\"10.17912/micropub.biology.001236\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The <i>E.3.3</i> mutation was generated in a Flp/FRT EMS screen for conditional mutations that cause growth and developmental defects in a genetic background that blocks apoptosis. The mutations were conditional, based on the <i>Dark <sup>82</sup></i> allele being present on the starting chromosome, and blocking canonical apoptosis in a homozygous state. The <i>E.3.3</i> mosaic eyes exhibit defects in eye development including patches of rough eye and irregular surface structure. Whole Genome Sequencing and complementation mapping revealed <i>E.3.3</i> as an allele of <i>prod</i> . Prod is a DNA-binding protein that binds satellite repeats and is involved in chromocenter formation during mitosis. Here we present a novel allele of <i>prod</i> , <i>prod <sup>E.3.3</sup></i> , that disrupts the functional region of the Prod protein resulting in disruption of typical eye structure, likely due to disruption of chromatid separation during development.</p>\",\"PeriodicalId\":74192,\"journal\":{\"name\":\"microPublication biology\",\"volume\":\"2024 \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11320118/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"microPublication biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.17912/micropub.biology.001236\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"microPublication biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17912/micropub.biology.001236","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
E.3.3突变是在Flp/FRT EMS筛选中产生的,目的是筛选出在阻断细胞凋亡的遗传背景下会导致生长和发育缺陷的条件突变。突变是有条件的,基于起始染色体上存在 Dark 82 等位基因,并在同源状态下阻断典型的细胞凋亡。E.3.3 马赛克眼表现出眼球发育缺陷,包括眼球粗糙斑块和不规则的表面结构。全基因组测序和互补图谱显示,E.3.3 是 Prod 的等位基因。Prod 是一种 DNA 结合蛋白,能与卫星重复序列结合,并参与有丝分裂过程中染色体中心的形成。在这里,我们发现了一个新的等位基因 prod E.3.3,它破坏了 Prod 蛋白的功能区,导致典型眼球结构的破坏,这可能是由于发育过程中染色体分离的破坏造成的。
Genetic Mapping of prod E.3.3 , a New Lethal Allele of prod.
The E.3.3 mutation was generated in a Flp/FRT EMS screen for conditional mutations that cause growth and developmental defects in a genetic background that blocks apoptosis. The mutations were conditional, based on the Dark 82 allele being present on the starting chromosome, and blocking canonical apoptosis in a homozygous state. The E.3.3 mosaic eyes exhibit defects in eye development including patches of rough eye and irregular surface structure. Whole Genome Sequencing and complementation mapping revealed E.3.3 as an allele of prod . Prod is a DNA-binding protein that binds satellite repeats and is involved in chromocenter formation during mitosis. Here we present a novel allele of prod , prod E.3.3 , that disrupts the functional region of the Prod protein resulting in disruption of typical eye structure, likely due to disruption of chromatid separation during development.