首页> 外文期刊>Evolution: International Journal of Organic Evolution >Multiple Origins Of Sex Chromosome Fusions Correlated With Chiasma Localization In Habronattus Jumping Spiders (Araneae: Salticidae)
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Multiple Origins Of Sex Chromosome Fusions Correlated With Chiasma Localization In Habronattus Jumping Spiders (Araneae: Salticidae)

机译:性状染色体融合的多种起源与Habronattus跳跃蜘蛛中的嵌合体定位相关(Araneae:Salticidae)

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Entelegyne spiders rarely show fusions yielding neo-Y chromosomes, which M. J. D. White attributed to a constraint in spiders, namely their proximal chiasma localization acting to upset meiotic segregation in males with fusions. Of the 75 taxa of Habronattus and outgroups studied, 47 have X_1X_20 sex chromosomes in males, 10 have X_1X_2Y, 15 have X_1X_2X_3Y, 2 have X0, and one has both X_1X_20 and X_1X_2X_3Y. Chromosome numbers and behavior suggest neo-Ys formed by an autosome-X fusion to make X_1X_2Y, with a second fusion to an autosome to make X_1X_2X_3Y. Phylogeny shows at least 8-15 gains (or possibly some losses) of neo-Y (i.e., X-autosome fusions), a remarkable number for such a small clade. In contrast to the many X-autosome fusions, at most one autosome-autosome fusion is indicated. Origins of neo-Y are correlated significantly with distal localization of chiasmata, supporting White's hypothesis that evolution of neo-Y systems is facilitated by looser pairing (distal chiasmata) at meiosis. However, an alternative (or contributing) explanation for the correlation is that X-autosome fusions were selected to permit isolation of male-favored alleles to the neo-Y chromosome, aided by distal chiasmata limiting recombination. This intralocus sexual conflict hypothesis could explain both the many X-autosome fusions, and the stunning complexity of male Habronattus courtship displays.
机译:Entelegyne蜘蛛很少显示融合产生新Y染色体的现象,M。J. D. White将其归因于蜘蛛的限制,即它们的近端横as定位使融合后的雄性减数分裂分离起作用。在所研究的Habronattus的75个分类群中,有47个具有X_1X_20个性别染色体,男性10个具有X_1X_2Y,15个具有X_1X_2X_3Y,2个具有X0,一个具有X_1X_20和X_1X_2X_3Y。染色体数目和行为表明,常染色体X融合形成的Neo-Y产生X_1X_2Y,而常染色体第二次融合形成X_1X_2X_3Y。系统发育学表明,至少有8-15个neo-Y(即X-常染色体融合体)获得(或可能有一些损失),对于这么小的进化枝来说,这是一个可观的数目。与许多X-常染色体融合体相反,指示最多一种常染色体-常染色体融合体。 Neo-Y的起源与横纹肌的远侧定位显着相关,支持怀特的假说,减数分裂时的松散配对(远侧横纹)促进了Neo-Y系统的进化。但是,这种相关性的另一种(或有助于性的)解释是,选择X-常染色体融合体以允许在远端Chismata限制重组的帮助下将雄性偏爱的等位基因分离到neo-Y染色体上。这种场所内性冲突假说既可以解释许多X常染色体融合,也可以解释雄性Habronattus求爱显示的惊人复杂性。

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