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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Deletion analysis of the selfish B chromosome, Paternal Sex Ratio (PSR), in the parasitic wasp Nasonia vitripennis.
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Deletion analysis of the selfish B chromosome, Paternal Sex Ratio (PSR), in the parasitic wasp Nasonia vitripennis.

机译:寄生黄蜂Nasonia vitripennis中自私的B染色体父本性别比(PSR)的缺失分析。

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Paternal Sex Ratio (PSR) is a "selfish" B chromosome in the parasitoid wasp Nasonia vitripennis. It is transmitted via sperm, but causes supercondensation and destruction of the paternal chromosomes in early fertilized eggs. Because this wasp has haplodiploid sex determination, the effect of PSR is to convert diploid (female) eggs into haploid (male) eggs that carry PSR. Characterizing its genetic structure is a first step toward understanding mechanisms of PSR action. The chromosome is largely heterochromatic and contains several tandemly repeated DNA sequences that are not present on the autosomes. A deletion analysis of PSR was performed to investigate organization of repeats and location of functional domains causing paternal chromosome destruction. Deletion profiles using probes to PSR-specific repetitive DNA indicate that most repeats are organized in blocks on the chromosome. This study shows that the functional domains of PSR can be deleted, resulting in nonfunctional PSR chromosomes that are transmitted to daughters. A functional domain may be linked with the psr22 repeat, but function may also depend on abundance of PSR-specific repeats on the chromosome. It is hypothesized that the repeats act as a "sink" for a product required for proper paternal chromosome processing. Almost all deletion chromosomes remained either functional of nonfunctional in subsequent generations following their creation. One chromosome was exceptional in that it reverted from nonfunctionality to functionality in one lineage. Transmission rates of nonfunctional deletion chromosomes were high through haploid males, but low through diploid females.
机译:父本性别比(PSR)是寄生蜂黄蜂Nasonia vitripennis中的“自私” B染色体。它通过精子传播,但会导致早期受精卵中父本染色体的超浓缩和破坏。由于该黄蜂具有单倍体性别决定性,因此PSR的作用是将二倍体(雌性)卵转化为携带PSR的单倍体(雄性)卵。表征其遗传结构是了解PSR作用机制的第一步。染色体主要是异色的,并包含常染色体上不存在的几个串联重复的DNA序列。进行了PSR的缺失分析,以研究重复序列的组织和引起父系染色体破坏的功能域的位置。使用针对PSR特异性重复DNA的探针进行的缺失分析表明,大多数重复序列均以染色体上的嵌段形式组织。这项研究表明,PSR的功能域可以被删除,导致无功能的PSR染色体被传递给子代。功能域可能与psr22重复序列相连,但功能也可能取决于染色体上PSR特异性重复序列的丰度。假设该重复序列充当适当父系染色体加工所需产品的“沉”。几乎所有的缺失染色体在其创建后的后代中都保持着功能性或非功能性。一条染色体是例外,因为它在一个谱系中从非功能性恢复为功能性。非功能性缺失染色体的传播率在单倍体雄性中较高,而在二倍体雌性中较低。

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