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The I.3.2 developmental mutant has a single nucleotide deletion in the gene centromere identifier .
- Source :
-
MicroPublication biology [MicroPubl Biol] 2022 Oct 25; Vol. 2022. Date of Electronic Publication: 2022 Oct 25 (Print Publication: 2022). - Publication Year :
- 2022
-
Abstract
- 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.<br /> (Copyright: © 2022 by the authors.)
Details
- Language :
- English
- ISSN :
- 2578-9430
- Volume :
- 2022
- Database :
- MEDLINE
- Journal :
- MicroPublication biology
- Publication Type :
- Academic Journal
- Accession number :
- 36389120
- Full Text :
- https://doi.org/10.17912/micropub.biology.000653