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

Authors :
Evans CJ
Bieser KL
Acevedo-Vasquez KS
Augustine EJ
Bowen S
Casarez VA
Feliciano VI
Glazier A
Guinan HR
Hallman R
Haugan E
Hehr LA
Hunnicutt SN
Leifer I
Mauger M
Mauger M
Melendez NY
Milshteyn L
Moore E
Nguyen SA
Phanphouvong SC
Pinal DM
Pope HM
Salinas MM
Shellin M
Small I
Yeoh NC
Yokomizo AMK
Kagey JD
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