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The I.3.2 developmental mutant has a single nucleotide deletion in the gene centromere identifier

The mutation I.3.2 was previously identified in a FLP/FRT screen of chromosome 2R for conditional growth regulators. Here we report the phenotypic characterization and genetic mapping of I.3.2 by undergraduate students participating in Fly-CURE, a pedagogical program that teaches the science of gene...

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Autores principales: Evans, Cory J., Bieser, Kayla L., Acevedo-Vasquez, Katherine S., Augustine, Emyli J., Bowen, Skyler, Casarez, Veronica A., Feliciano, Vanessa I., Glazier, Ashley, Guinan, Haley R., Hallman, Randy, Haugan, Elizabeth, Hehr, Lauren A., Hunnicutt, Shawna N., Leifer, Isabella, Mauger, Meaghan, Mauger, Morgan, Melendez, Norma Y., Milshteyn, Larry, Moore, Eric, Nguyen, Sarah A., Phanphouvong, Sierra C., Pinal, David M., Pope, Hailee M., Salinas, Mark-Brandon M., Shellin, Matthew, Small, Ivana, Yeoh, Neelufar C., Yokomizo, Alexandra M.K., Kagey, Jacob D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644223/
https://www.ncbi.nlm.nih.gov/pubmed/36389120
http://dx.doi.org/10.17912/micropub.biology.000653
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author Evans, Cory J.
Bieser, Kayla L.
Acevedo-Vasquez, Katherine S.
Augustine, Emyli J.
Bowen, Skyler
Casarez, Veronica A.
Feliciano, Vanessa I.
Glazier, Ashley
Guinan, Haley R.
Hallman, Randy
Haugan, Elizabeth
Hehr, Lauren A.
Hunnicutt, Shawna N.
Leifer, Isabella
Mauger, Meaghan
Mauger, Morgan
Melendez, Norma Y.
Milshteyn, Larry
Moore, Eric
Nguyen, Sarah A.
Phanphouvong, Sierra C.
Pinal, David M.
Pope, Hailee M.
Salinas, Mark-Brandon M.
Shellin, Matthew
Small, Ivana
Yeoh, Neelufar C.
Yokomizo, Alexandra M.K.
Kagey, Jacob D.
author_facet Evans, Cory J.
Bieser, Kayla L.
Acevedo-Vasquez, Katherine S.
Augustine, Emyli J.
Bowen, Skyler
Casarez, Veronica A.
Feliciano, Vanessa I.
Glazier, Ashley
Guinan, Haley R.
Hallman, Randy
Haugan, Elizabeth
Hehr, Lauren A.
Hunnicutt, Shawna N.
Leifer, Isabella
Mauger, Meaghan
Mauger, Morgan
Melendez, Norma Y.
Milshteyn, Larry
Moore, Eric
Nguyen, Sarah A.
Phanphouvong, Sierra C.
Pinal, David M.
Pope, Hailee M.
Salinas, Mark-Brandon M.
Shellin, Matthew
Small, Ivana
Yeoh, Neelufar C.
Yokomizo, Alexandra M.K.
Kagey, Jacob D.
author_sort Evans, Cory J.
collection PubMed
description The mutation I.3.2 was previously identified in a FLP/FRT screen of chromosome 2R for conditional growth regulators. Here we report the phenotypic characterization and genetic mapping of I.3.2 by undergraduate students participating in Fly-CURE, a pedagogical program that teaches the science of genetics through a classroom research experience. We find that creation of I.3.2 cell clones in the developing eye-antennal imaginal disc causes a headless adult phenotype, suggestive of both autonomous and non-autonomous effects on cell growth or viability. We also identify the I.3.2 mutation as a loss-of-function allele of the gene centromere identifier ( cid ), which encodes centromere-specific histone H3 variant critical for chromosomal segregation.
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spelling pubmed-96442232022-11-15 The I.3.2 developmental mutant has a single nucleotide deletion in the gene centromere identifier Evans, Cory J. Bieser, Kayla L. Acevedo-Vasquez, Katherine S. Augustine, Emyli J. Bowen, Skyler Casarez, Veronica A. Feliciano, Vanessa I. Glazier, Ashley Guinan, Haley R. Hallman, Randy Haugan, Elizabeth Hehr, Lauren A. Hunnicutt, Shawna N. Leifer, Isabella Mauger, Meaghan Mauger, Morgan Melendez, Norma Y. Milshteyn, Larry Moore, Eric Nguyen, Sarah A. Phanphouvong, Sierra C. Pinal, David M. Pope, Hailee M. Salinas, Mark-Brandon M. Shellin, Matthew Small, Ivana Yeoh, Neelufar C. Yokomizo, Alexandra M.K. Kagey, Jacob D. MicroPubl Biol New Finding The mutation I.3.2 was previously identified in a FLP/FRT screen of chromosome 2R for conditional growth regulators. Here we report the phenotypic characterization and genetic mapping of I.3.2 by undergraduate students participating in Fly-CURE, a pedagogical program that teaches the science of genetics through a classroom research experience. We find that creation of I.3.2 cell clones in the developing eye-antennal imaginal disc causes a headless adult phenotype, suggestive of both autonomous and non-autonomous effects on cell growth or viability. We also identify the I.3.2 mutation as a loss-of-function allele of the gene centromere identifier ( cid ), which encodes centromere-specific histone H3 variant critical for chromosomal segregation. Caltech Library 2022-10-25 /pmc/articles/PMC9644223/ /pubmed/36389120 http://dx.doi.org/10.17912/micropub.biology.000653 Text en Copyright: © 2022 by the authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle New Finding
Evans, Cory J.
Bieser, Kayla L.
Acevedo-Vasquez, Katherine S.
Augustine, Emyli J.
Bowen, Skyler
Casarez, Veronica A.
Feliciano, Vanessa I.
Glazier, Ashley
Guinan, Haley R.
Hallman, Randy
Haugan, Elizabeth
Hehr, Lauren A.
Hunnicutt, Shawna N.
Leifer, Isabella
Mauger, Meaghan
Mauger, Morgan
Melendez, Norma Y.
Milshteyn, Larry
Moore, Eric
Nguyen, Sarah A.
Phanphouvong, Sierra C.
Pinal, David M.
Pope, Hailee M.
Salinas, Mark-Brandon M.
Shellin, Matthew
Small, Ivana
Yeoh, Neelufar C.
Yokomizo, Alexandra M.K.
Kagey, Jacob D.
The I.3.2 developmental mutant has a single nucleotide deletion in the gene centromere identifier
title The I.3.2 developmental mutant has a single nucleotide deletion in the gene centromere identifier
title_full The I.3.2 developmental mutant has a single nucleotide deletion in the gene centromere identifier
title_fullStr The I.3.2 developmental mutant has a single nucleotide deletion in the gene centromere identifier
title_full_unstemmed The I.3.2 developmental mutant has a single nucleotide deletion in the gene centromere identifier
title_short The I.3.2 developmental mutant has a single nucleotide deletion in the gene centromere identifier
title_sort the i.3.2 developmental mutant has a single nucleotide deletion in the gene centromere identifier
topic New Finding
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644223/
https://www.ncbi.nlm.nih.gov/pubmed/36389120
http://dx.doi.org/10.17912/micropub.biology.000653
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