Abstract

Maintenance of the chromosomal copy number over generations and recombination between homologous chromosomes are hallmarks of meiotic cell division. This genetic exchange that take place during gamete formation leads to genetic diversity, the main driving force behind natural selection. Formation of chiasmata, the physical link between homologous chromosomes during meiosis, is a requisite for recombination. In addition, chiasmata also aid in proper segregation of homologous chromosomes and has a major impact on reproductive fitness. Given these facts it is intriguing that many insect species have forgone the need for genetic exchange between homologous chromosomes during meiosis. Geneticists for several decades knew that meiotic crossover and recombination is absent in Drosophila males and some female lepidopterans, a condition termed achiasmy. However, a good understanding of the mechanisms that cause achiasmy and the evolutionary benefits of achiasmy is currently lacking. In this article we will discuss possible genetic and molecular basis of achiasmy in male Drosophila.

Highlights

  • Meiotic cell division, an essential step in sexual reproduction, helps in the segregation of homologous chromosomes and sister chromatids

  • A crucial task for meiotic cell division is the maintenance of recombination mediated genetic variability (Hunter, 2015)

  • An added advantage of Achiasmy in male Drosophila meiotic recombination is that the chiasmata formation during crossover helps in proper alignment and segregation of chromosomes (Carpenter, 1994)

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Summary

Introduction

An essential step in sexual reproduction, helps in the segregation of homologous chromosomes and sister chromatids. An added advantage of Achiasmy in male Drosophila meiotic recombination is that the chiasmata formation during crossover helps in proper alignment and segregation of chromosomes (Carpenter, 1994). Drosophila females, like the majority of sexually reproducing organisms, generate crossovers between homologous chromosomes to direct segregation at the first meiotic division (Lindsley and Sandler, 1977; Puro and Nokkala, 1977; Lin et al, 1981; Orr-Weaver, 1995; Lichten, 2001; McKim et al, 2002; Figure 1).

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