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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Caltech Library
2022
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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. |
format | Online Article Text |
id | pubmed-9644223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Caltech Library |
record_format | MEDLINE/PubMed |
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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