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[因畸变导致的不育]

[Sterility due to aberrations].

作者信息

Dennhöfer L

机构信息

Institut für Entwicklungsphysiologie der Universität zu Köln, Germany.

出版信息

Theor Appl Genet. 1974 Jan;44(7):311-23. doi: 10.1007/BF00275869.

Abstract

A decrease of fertility can be caused by chromosomal aberrations of two different types: 1) Inversions and transpositions Aneuploid gametes will only be formed, if crossingover had happened between the breakpoints. A possible regulation against this sterility is avoiding any crossingover in the organism. Especially mechanisms in oogenesis and spermatogenesis are developed against paracentric inversions only. 2) Reciprocal translocations Aneuploid gametes are the result of adjacent segregation of the chromosomes involved in the translocation. The percentage of sterility is correlated with the relation of alternate and adjacent segregation. At random segregation results a relation of 2∶4 between euploid and aneuploid gametes resp. 66% sterility. But in literature there are described all possible relations between euploid and aneuploid gametes; this not only in different genera but also in populations of a species (per example in crossing experiments). These facts, especially the results of crossing experiments beget the hypothesis, that segregation of the chromosomes involved in a translocation is under strict genetic control. We postulate, that it is attributable to a single, Mendelian factor, called "sg". This factor exists in a series of multiple alleles causing different relations between alternate and adjacent segregation. The allelomorph causing a higher fertility is dominant over the allelomorph, producing less euploid gametes. The percentage of sterility resp. fertility due to a translocation is not constant, but can be changed by mutual events. The individuum possessing the allele for more fertile gametes - without respect whether homo- or heterozygotous - will produce more offspring than another individuum with lower regulating alleles. So the alleles for sterility will be lost in the course of evolution. Finally, only individuals of a species with complete fertility (sg(4)/sg(4)) will survive in spite of segmental interchange (like Oenothera ssp., Periplaneta americana etc.). These mechanisms of regulation against sterility due to chromosomal aberrations are of interest in view of pest control with genetic methods.

摘要

生育力下降可能由两种不同类型的染色体畸变引起

1)倒位和易位 只有在断点之间发生交叉时才会形成非整倍体配子。针对这种不育的一种可能调节方式是避免生物体中发生任何交叉。特别是在卵子发生和精子发生过程中仅针对臂内倒位形成了相应机制。2)相互易位 非整倍体配子是易位所涉及染色体相邻分离的结果。不育的百分比与交替分离和相邻分离的比例相关。随机分离时,整倍体和非整倍体配子的比例为2∶4,不育率为66%。但文献中描述了整倍体和非整倍体配子之间所有可能的比例关系;这不仅在不同属中存在,在一个物种的种群中也存在(例如在杂交实验中)。这些事实,尤其是杂交实验的结果引发了这样的假设,即易位所涉及染色体的分离受到严格的遗传控制。我们假设,这归因于一个单一的孟德尔因子,称为“sg”。这个因子存在一系列复等位基因,导致交替分离和相邻分离之间的不同比例关系。导致更高生育力的等位基因相对于产生较少整倍体配子的等位基因是显性的。由于易位导致的不育或生育力百分比不是恒定的,而是可以通过相互作用的事件改变。拥有更能育配子等位基因的个体——无论其是纯合还是杂合——将比具有较低调节等位基因的另一个个体产生更多后代。因此,不育等位基因将在进化过程中丢失。最终,尽管存在片段交换(如月见草属物种、美洲大蠊等),一个物种中只有具有完全生育力(sg(4)/sg(4))的个体才能存活。鉴于采用遗传方法进行害虫防治,这些针对染色体畸变导致不育的调节机制具有重要意义。

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