M. Steinemann et S. Steinemann, ENIGMA OF Y-CHROMOSOME DEGENERATION - NEO-Y AND NEO-X CHROMOSOMES OF DROSOPHILA-MIRANDA A MODEL FOR SEX-CHROMOSOME EVOLUTION, Genetica, 103, 1998, pp. 409-420
Y chromosome degeneration is characterized by structural changes in th
e chromosome architecture and expansion of genetic inertness along the
Y chromosome. It is generally assumed that the heteromorphic sex chro
mosome pair has developed from a pair of homologues. Several models ha
ve been suggested. We use the unique situation of the secondary sex ch
romosome pair, neo-Y and neo-X(X2), in Drosophila miranda to analyze m
olecular mechanisms involved in the evolutionary processes of Y chromo
some degeneration. Due to the fusion of one of the autosomes to the Y
chromosome (about 2 Mya), a neo-Y chromosome and a neo-X chromosome, d
esignated X2, were formed. Thus, formerly autosomal genes are inherite
d now on a pair of sex chromosomes in D. miranda. Analyzing DNA sequen
ces from the X2 and neo-Y region, we observed a massive accumulation o
f DNA insertions on the neo-Y chromosome. From the analysis of several
insertion elements, we present compelling evidence that the first ste
p in Y chromosome degeneration is driven by the accumulation of transp
osable elements, especially retrotransposons. An enrichment of these e
lements along an evolving Y chromosome could account for the switch fr
om a euchromatic into a heterochromatic chromatin structure.