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Advances in Clinical Toxicology Research Article 3 min read

Polytene Chromosomes as a Genotoxicology Tool

<p>Ayla Karatas*</p>*
* Corresponding author
ISSN: 2577-4328  10.23880/act-16000117  Received: September 27, 2017  Published: October 02, 2017
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Abstract

&nbsp;It is not possible to visualize the interphase chromosomes with light microscopy; however, polytene chromosomes are giant interphase chromosomes visible under light microscopy. Therefore, polytene chromosomes of Drosophila melanogaster are unique materials for the observation and analysis of the genome and genetic organization of chromosomes in the interphase stage. Polytene chromosomes form through the sequential replication of the chromosomes of the diploid nucleus division of the cytoplasm following the replication. This way, a chromosome 70 to 110 time thicker than a typical metaphase chromosome and observable with light microscopy, appears. This interesting polyteny occurs within the cellular cycle, during the mid-phases of Drosophila melanogaster's embryogenesis under ecdysone, which is particularly important for the development of larva. Investigation of every aspect of polytene chromosomes is very useful for the analysis of chromosomal organization and genome as a whole.&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;

Editorial

It is not possible to visualize the interphase chromosomes with light microscopy; however, polytene chromosomes are giant interphase chromosomes visible under light microscopy. Therefore, polytene chromosomes of Drosophila melanogaster are unique materials for the observation and analysis of the genome and genetic organization of chromosomes in the interphase stage. Polytene chromosomes form through the sequential replication of the chromosomes of the diploid nucleus division of the cytoplasm following the replication. This way, a chromosome 70 to 110 time thicker than a typical metaphase chromosome and observable with light microscopy, appears. This interesting polyteny occurs within the cellular cycle, during the mid-phases of Drosophila melanogaster's embryogenesis under ecdysone, which is particularly important for the development of larva. Investigation of every aspect of polytene chromosomes is very useful for the analysis of chromosomal organization and genome as a whole [1, 2]. The most detailed maps of the polytene chromosomes in salivary glands of Drosophila melanogaster were created by Bridges using light microscopy in 1930s and 1940s [3]. The stiffly packed and dense dark areas are called bands, and lighter and less dense areas are called interbands. Localization of RNA polymerase II and related transcription factors on interbands shows that active genes tend to locate on these band areas [4]. Furthermore, areas in the interbands that are swelled more densely and observed as puffed areas are called puffs. Typical feature of puff areas is that they are rather active gene areas with RNA synthesis in higher rates as compared to the other areas of the interphase chromosomes. So, model, sequence and timing of puffing in the polytene chromosomes can be considered as

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@article{ayla2017,
  title   = {Polytene Chromosomes as a Genotoxicology Tool},
  author  = {Ayla Karatas},
  journal = {Advances in Clinical Toxicology},
  year    = {2017},
  volume  = {2},
  number  = {1},
  doi     = {10.23880/act-16000117}
}
Ayla Karatas (2017). Polytene Chromosomes as a Genotoxicology Tool. Advances in Clinical Toxicology, 2(1). https://doi.org/10.23880/act-16000117
TY  - JOUR
TI  - Polytene Chromosomes as a Genotoxicology Tool
AU  - Ayla Karatas
JO  - Advances in Clinical Toxicology
PY  - 2017
VL  - 2
IS  - 1
DO  - 10.23880/act-16000117
ER  -