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首页> 外文期刊>G3: Genes, Genomes, Genetics >Cold Fusion: Massive Karyotype Evolution in the Antarctic Bullhead Notothen Notothenia coriiceps
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Cold Fusion: Massive Karyotype Evolution in the Antarctic Bullhead Notothen Notothenia coriiceps

机译:冷聚变:南极牛头诺丁氏夜蛾皮损的大规模核型型演变。

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Half of all vertebrate species share a series of chromosome fusions that preceded the teleost genome duplication (TGD), but we do not understand the causative evolutionary mechanisms. The “Robertsonian-translocation hypothesis” suggests a regular fusion of each ancestral acro- or telocentric chromosome to just one other by centromere fusions, thus halving the karyotype. An alternative “genome-stirring hypothesis” posits haphazard and repeated fusions, inversions, and reciprocal and nonreciprocal translocations. To study large-scale karyotype reduction, we investigated the decrease of chromosome numbers in Antarctic notothenioid fish. Most notothenioids have 24 haploid chromosomes, but bullhead notothen ( Notothenia coriiceps ) has 11. To understand mechanisms, we made a RAD-tag meiotic map with ~10,000 polymorphic markers. Comparative genomics aligned about a thousand orthologs of platyfish and stickleback genes along bullhead chromosomes. Results revealed that 9 of 11 bullhead chromosomes arose by fusion of just two ancestral chromosomes and two others by fusion of three ancestral chromosomes. All markers from each ancestral chromosome remained contiguous, implying no inversions across fusion borders. Karyotype comparisons support a history of: (1) Robertsonian fusions of 22 ancestral chromosomes in pairs to yield 11 fused plus two small unfused chromosomes, like N. angustata ; (2) fusion of one of the remaining two ancestral chromosomes to a preexisting fused pair, giving 12 chromosomes like N. rossii ; and (3) fusion of the remaining ancestral chromosome to another fused pair, giving 11 chromosomes in N. coriiceps . These results raise the question of what selective forces promoted the systematic fusion of chromosomes in pairs and the suppression of pericentric inversions in this lineage, and provide a model for chromosome fusions in stem teleosts.
机译:所有脊椎动物中有一半共享在硬骨基因组复制(TGD)之前的一系列染色体融合,但是我们不了解其致病性进化机制。 “罗伯逊易位假说”提出通过着丝粒融合将每个祖先的顶体或端中心染色体规则地融合在一起,从而使核型减半。另一种“搅动基因组的假设”提出了偶然性和反复融合,倒置以及相互和非相互易位的假设。为了研究大规模的核型减少,我们调查了南极类异戊二烯鱼的染色体数目减少。大多数类异戊二烯具有24个单倍体染色体,而牛头诺丁烯(Notothenia coriiceps)具有11个。为了解机理,我们绘制了一个RAD标签减数分裂图,该图具有10,000个多态性标记。比较基因组学沿牛头染色体排列了约一千个板鱼和棘背基因的直系同源基因。结果显示,11条牛头染色体中的9条仅通过融合两个祖先染色体而产生,另外两个通过融合三个祖先染色体而产生。每个祖先染色体上的所有标记都保持连续,这意味着融合边界没有倒置。染色体核型比较支持以下历史:(1)成对的22个祖先染色体的罗伯逊融合产生11个融合的染色体加上两个小的未融合的染色体,如N. angustata; (2)将剩余的两个祖先染色体之一融合到一个已存在的融合对中,得到12个染色体,如罗氏沼虾; (3)将剩余的祖先染色体融合到另一对融合的染色体上,从而在N. coriiceps中产生11条染色体。这些结果提出了一个问题,即哪些选择性力促进了成对染色体的系统融合以及该谱系中外周中心反转的抑制,并为茎硬骨鱼中的染色体融合提供了模型。

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