» Articles » PMID: 16020774

Highly Efficient Sex Chromosome Interchanges Produced by I-CreI Expression in Drosophila

Overview
Journal Genetics
Specialty Genetics
Date 2005 Jul 16
PMID 16020774
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

The homing endonuclease I-CreI recognizes a site in the gene encoding the 23S rRNA of Chlamydomonas reinhardtii. A very similar sequence is present in the 28S rRNA genes that are located on the X and Y chromosomes of Drosophila melanogaster. In this work we show that I-CreI expression in Drosophila is capable of causing induced DNA damage and eliciting cell cycle arrest. Expression also caused recombination between the X and Y chromosomes in the heterochromatic regions where the rDNA is located, presumably as a result of a high frequency of double-strand breaks in these regions. Approximately 20% of the offspring of males expressing I-CreI showed exceptional inheritance of X- and Y-linked markers, consistent with chromosome exchange at rDNA loci. Cytogenetic analysis confirmed the structures of many of these products. Exchange between the X and Y chromosomes can be induced in males and females to produce derivative-altered Y chromosomes, attached-XY, and attached-X chromosomes. This method has advantages over the traditional use of X rays for generating X-Y interchanges because it is very frequent and it generates predictable products.

Citing Articles

Acentric chromosome congression and alignment on the metaphase plate via kinetochore-independent forces.

Vicars H, Mills A, Karg T, Sullivan W Genetics. 2024; 229(2).

PMID: 39552081 PMC: 11796462. DOI: 10.1093/genetics/iyae188.


Under the magnifying glass: The ups and downs of rDNA copy number.

Kindelay S, Maggert K Semin Cell Dev Biol. 2022; 136:38-48.

PMID: 35595601 PMC: 9976841. DOI: 10.1016/j.semcdb.2022.05.006.


Dynamic localization of DNA topoisomerase I and its functional relevance during Drosophila development.

Huang W, Liu Z, Rong Y G3 (Bethesda). 2021; 11(9).

PMID: 34544118 PMC: 8661406. DOI: 10.1093/g3journal/jkab202.


DNase II mediates a parthanatos-like developmental cell death pathway in Drosophila primordial germ cells.

Tarayrah-Ibraheim L, Maurice E, Hadary G, Ben-Hur S, Kolpakova A, Braun T Nat Commun. 2021; 12(1):2285.

PMID: 33863891 PMC: 8052343. DOI: 10.1038/s41467-021-22622-1.


Kinetochore-independent mechanisms of sister chromosome separation.

Vicars H, Karg T, Warecki B, Bast I, Sullivan W PLoS Genet. 2021; 17(1):e1009304.

PMID: 33513180 PMC: 7886193. DOI: 10.1371/journal.pgen.1009304.


References
1.
Bridges C . Non-Disjunction as Proof of the Chromosome Theory of Heredity. Genetics. 1916; 1(1):1-52. PMC: 1193653. DOI: 10.1093/genetics/1.1.1. View

2.
Hadorn E, Gsell R, Schultz J . Stability of a position-effect variegation in normal and transdetermined larval blastemas from Drosophila melanogaster. Proc Natl Acad Sci U S A. 1970; 65(3):633-7. PMC: 282953. DOI: 10.1073/pnas.65.3.633. View

3.
Neuhaus M . Additional Data on Crossing over between X and Y Chromosomes in Drosophila Melanogaster. Genetics. 1937; 22(3):333-9. PMC: 1208967. DOI: 10.1093/genetics/22.3.333. View

4.
Royou A, Macias H, Sullivan W . The Drosophila Grp/Chk1 DNA damage checkpoint controls entry into anaphase. Curr Biol. 2005; 15(4):334-9. DOI: 10.1016/j.cub.2005.02.026. View

5.
Robbins L . Genetically induced mitotic exchange in the heterochromatin of Drosophila melanogaster. Genetics. 1981; 99(3-4):443-59. PMC: 1214513. DOI: 10.1093/genetics/99.3-4.443. View