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Adams, J. R.

Publications and source records attributed to Adams, J. R..

2 recordsLinked to original sources

Little heterosis found in Diploid Hybrid Potato

Hybrid potato breeding has become a novel alternative to con-ventional potato breeding allowing breeders to overcome intractable barriers (e.g. tetrasomic inheritance, masked deleterious alleles, obligate clonal propagation) with the benefit of seed-based propagule, flexible population design, and the potential of hybrid vigour. Until now, however, no formal inquiry has adequately examined the relevant genetic components for complex traits in hybrid potato populations. In this present study, we use a two-step modelling approach to estimate the relevant variance components to assess the magnitude of the general and specific combining abilities (GCA and SCA, respectively) in diploid hybrid potato (DHP). SCA effects were identified for all yield components studied here warranting evidence of non-additive genetic effects in hybrid potato yield. However, the estimated GCA effects were on average two times larger than their respective SCA quantile across all yield phenotypes. Tuber number GCAs and SCAs were found to be highly correlated with total yields genetic components. Tuber volume appearing under-selected in this population. The prominence of additive effects found for all traits presents evidence that breeders can perform hybrid potato evaluation using the mid-parent value alone. Heterotic vigour stands be useful in bolstering simpler traits but this will be very dependent on the target market of a population. This study represents the first diallel analysis of its kind in diploid potato using material derived from a commercial hybrid breeding programme.

genetics↗

Development of a drug repressible β-catenin mutant mouse to examine effect of activated β-catenin signaling on long-term maintenance of mammary tumor growth

Stabilized {beta}-catenin expression is a well described initiator of mammary tumorigenesis in the mouse and elevated nuclear expression of this protein has been observed in human triple-negative tumor samples. However, the importance of stabilized {beta}-catenin to continued tumor growth after initiation, and in the context of other driver mutations, has yet to be elucidated. To ascertain the importance of stabilized {beta}-catenin after tumor initiation, we generated a novel transgenic mouse model, utilizing the tet-off system, to control expression of a stabilized mutant of {beta}-catenin. Pups from early litters carrying one allele of regulatable stabilized {beta}-catenin at the Rosa26 locus, but not targeted by Cre, were smaller in size compared with wildtype littermates and also developed skin lesions, requiring euthanasia. Maintenance of breeding cages on doxycycline chow allowed for healthy transgenic pups to survive past 3 weeks of age and 6 animal cohorts were established. We used two different mammary Cre strains, WAP-Cre and MMTV-NLST-Cre, crossed with regulatable, stabilized {beta}-catenin (bcatFL) animals, as well as animals expressing mutated p53-R270H. While mammary tumors developed in animals expressing Cre-targeted regulatable bcatFL, the penetrance and growth kinetics were lower than observed with other mammary mouse models expressing stabilized {beta}-catenin. Since fewer animals developed tumors, we focused analysis on the effect of turning off stabilized {beta}-catenin expression following tumor initiation. In the animals examined, a delay in tumor growth, but not regression, was observed in animals expressing Cretargeted bcatFL as well as those expressing both bcatFL and p53-R270H. These results indicate that in a less aggressive {beta}-catenin model, additional mutations likely provide independence from the initiating event.

cancer biology↗