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144<br />

6. DO ANY SPECIES BOUNDARIES....<br />

Noteworthy, all enzymatic loci but Sod1, deviating from the Mendelian model of inheritance in<br />

the interspecific population BR3 x NZ15, were tightly linked with transposon sequences.<br />

6.3.4. Inheritance of selected traits in intra- and interspecific crosses<br />

Seedling root fluorescence (SRF)<br />

Seedling root fluorescence (SRF) segregated in both interspecific F 2<br />

populations (BR3<br />

x NZ15 and HU5 x BO2) and in the F 2<br />

population of L. multiflorum, VA7 x AS17. Unsurprisingly,<br />

no segregation was observed in the L. perenne F 2<br />

population, KY20 x BB6, which was<br />

derived from nonfluorescent parents (Table 6.11). The roots of the F 1<br />

hybrid did not fluoresce<br />

as well.<br />

Segregation of seedling root fluorescence was consisted with the monogenic dominant<br />

mode of inheritance in the L. multiflorum population and in the F 2<br />

derived from the interspecific<br />

cross between L. perenne and L. multiflorum, HU5 x BO2. However, the significant<br />

deviation from the expected 3:1 ratio was observed in the second interspecific population<br />

derived from the cross between L. multiflorum and L. perenne, BR3 x NZ15. By contrary, the<br />

segregation of seedling root fluorescence in this population was in agreement with the 9:7<br />

ratio typical of two complementary genes.<br />

A report from genetic mapping studies in the L. multiflorum x L. perenne population,<br />

BR3 x NZ15 provided other evidences that at least two genes may be responsible for the<br />

SRF character. Two regions were identified on the first linkage group (Figure 6.5A). The<br />

first locus was located on the proximal part of LG1 and it was tightly linked with Lolcopia2<br />

marker Lc2Pat22 (1.3 cM). It was also located more than 30 cM away from Est4 locus. This<br />

locus was further assigned as SRF1 with respective alleles, SRF1 as dominant and srf1 as<br />

recessive. The second one, further described as SRF2 with dominant SRF2 and recessive<br />

srf2 alleles, mapped on the same linkage group but in the distal part, in about 3.4 cM away<br />

from of a small cluster of three AFLP markers, McacEaac32, McaaEact15 and MctgEaac22.<br />

In proximity to this region, the insertion site of Tpo1 transposon (TpPat41) was found and<br />

enzymatic locus, Pgdh1 encoding phosphogluconate dehydrogenase (within 9 cM). Appar-

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