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A criticism of the value of midparent in polyploidization.

机译:对中倍体在多倍体化中的价值的批评。

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摘要

The hypothesis of genetic additivity states that the effects of different alleles, or different genes, add up to produce the phenotype. When considering the F1 progeny of a cross, the hypothesis of additivity of the genetic dosages provided by the parents is tested against the mid-parent value (MPV), which is the average of parental phenotypes and represents the reference value for genetic additivity. Non-additive effects (genetic interactions) are typically measured as deviations from MPV. Recently, however, the use of MPV has been directly transposed to the study of genetic additivity in newly synthesized plant polyploids, assuming that they should as well display mid-parent expression patterns for additive traits. It is shown here that this direct transposition is incorrect. It is suggested that, in neo-polyploids, mid-parent expression has to be reconsidered in terms of reduced genetic additivity. Homeostatic mechanisms are deemed to be the obvious ones responsible for this effect. Genomes are therefore ruled by negative epistasis, and heterosis in allopolyploids is due to a decreased interaction of the parental repressive systems. It is contended that focalizing on the right perspective has relevant theoretical consequences and makes the studies of neo-polyploids very important for our understanding of how genomes work.
机译:遗传可加性的假设指出,不同等位基因或不同基因的作​​用加在一起产生表型。当考虑杂交的F 1 后代时,针对亲本中值(MPV)检验由父母提供的遗传剂量的可加性假设,该值是亲本表型的平均值,表示遗传可加性的参考值。非累加效应(遗传相互作用)通常以与MPV的偏差来衡量。然而,最近,假设它们也应显示中性表现形式的加性,则将MPV的使用直接转用于新合成的植物多倍体中遗传可加性的研究。此处显示此直接转置不正确。建议在新的多倍体中,必须从降低遗传可加性的角度重新考虑中亲表达。稳态机制被认为是造成这种效应的明显机制。因此,基因组受阴性上位性的支配,同种多倍体的杂种优势是由于亲代抑制系统的相互作用降低。有人认为,专注于正确的观点具有相关的理论后果,并使新多倍体的研究对于我们对基因组如何工作的理解非常重要。

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