Zeller (1998) distinguished 7 hexaploids, assuming that A. byzantina was a subspecies of A. sativa, while in Loskutov's (2008) opinion, the genus consisted of 6 hexaploid species (A. fatua, A. sterilis, A. byzantina, A. sativa, A. occidentalis, and A. ludoviciana Dur.). Nevertheless, independent of taxonomy, the most notable representatives having species status that are recognized in the genus are A. sativa, A. fatua, and A. sterilis.The most common assumption is that the hexaploid species evolved from a single hexaploid ancestor followed by gain or loss of domestication genes (Leggett, 1992). Nevertheless, there are several concepts explaining the evolution of hexaploids. According to one, all hexaploid species moved from their Asian center predominantly westwards, and A. fatua occupied the northern and middle latitudes, while A. sterilis inhabited those to the south, reaching the western borders of the Mediterranean region (Malzev, 1930). Thus, A. sterilis might have originated from the same Asian center as A. fatua, but during its expansion differentiation took place. Nor is it obvious that A. sterilis L. or A. fatua L. is an ancestor of cultivated A. sativa. The former represents the oldest hexaploid. Study of oat chromosome translocations and correlation of that data with the geographic distribution of various forms demonstrated a high degree of genetic relationship among A. sativa L. and many forms of A. sterilis from eastern Anatolia (Zhou et al., 1999). A. sterilis is considered the ancestral form of the hexaploid oats (Jellen et al., 1993) due to the presence of the largest telomeric block in the long arm of 5C chromosome. Thomas (1992) claimed that A. sterilis generated fatua-type mutations that led to the emergence of A. fatua, from which weedy forms Abstract: Taxonomic relationships in Avena genus are not evident. Avena sativa L. might have originated either from Avena sterilis L. or Avena fatua L. Alternatively, it may have evolved independently during formation of the hexaploid form. A. fatua may have a different A genome than the other hexaploids. Studies performed with Ty1-copia retrotransposon probes demonstrated that this retrotransposon is present at low copy number in the C genome, while it is abundant in A, B, and D. The observed differences provide an opportunity for analyzing the putative origin of A. fatua as well as its relationships with other hexaploids. Two marker systems were applied. Retrotransposon-microsatellite amplified polymorphism (REMAP) was used to obtain evidence that the A genome of A. fatua has a different origin than the other hexaploids, and inter-simple sequence repeat (ISSR) was applied to screen for whole genome polymorphisms. The results tend to favor the hypothesis that A. sterilis could be the progenitor of A. sativa and A. fatua and showed that A. fatua could not have originated via cross with a maternal species having a different A genome than A. sterilis and A. sativa.