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检测果蝇中的染色体系统发生和倒位断点的重复利用。重新研究马滕斯集群。

Testing chromosomal phylogenies and inversion breakpoint reuse in Drosophila. The martensis cluster revisited.

机构信息

Departament de Genètica i de Microbiologia, Facultat de Biociències, Edifici C, Universitat Autònoma de Barcelona, 08193, Bellaterra, Barcelona, Spain.

出版信息

Chromosome Res. 2011 Feb;19(2):251-65. doi: 10.1007/s10577-011-9195-6. Epub 2011 Mar 11.

Abstract

The chromosomal relationships of the four martensis cluster species are among the most complex and intricate within the entire Drosophila repleta group, due to the so-called sharing of inversions. Here, we have revised these relationships using comparative mapping of bacterial artificial chromosome (BAC) clones on the salivary gland chromosomes. A physical map of chromosome 2 of Drosophila uniseta (one of the cluster members) was generated by in situ hybridization of 82 BAC clones from the physical map of the Drosophila buzzatii genome (an outgroup that represents the ancestral arrangement). By comparing the marker positions, we determined the number, order, and orientation of conserved chromosomal segments between chromosome 2 of D. buzzatii and D. uniseta. GRIMM software was used to infer that a minimum of five chromosomal inversions are necessary to transform the chromosome 2 of D. buzzatii into that of D. uniseta. Two of these inversions have been overlooked in previous cytological analyses. The five fixed inversions entail two breakpoint reuses because only nine syntenic segments and eight interruptions were observed. We tested for the presence of the five inversions fixed in D. uniseta in the other three species of the martensis cluster by in situ hybridization of eight breakpoint-bearing BAC clones. The results shed light on the chromosomal phylogeny of the martensis cluster, yet leave a number of questions open.

摘要

由于所谓的倒位共享,四芒沙潜蝇簇种的染色体关系是整个果蝇充实组中最复杂和错综复杂的。在这里,我们使用细菌人工染色体 (BAC) 克隆在唾液腺染色体上的比较作图修正了这些关系。通过对来自果蝇 buzzatii 基因组物理图谱(代表祖先排列的外群)的 82 个 BAC 克隆进行原位杂交,生成了果蝇 uniseta(簇成员之一)染色体 2 的物理图谱。通过比较标记位置,我们确定了 D. buzzatii 和 D. uniseta 染色体 2 之间保守染色体片段的数量、顺序和方向。使用 GRIMM 软件推断,至少需要五次染色体倒位才能将 D. buzzatii 的染色体 2 转化为 D. uniseta 的染色体 2。在之前的细胞学分析中忽略了其中两个倒位。这五个固定的倒位涉及两个断点重复使用,因为只观察到九个同线片段和八个中断。我们通过对八个带有断点的 BAC 克隆进行原位杂交,测试了 D. uniseta 中固定的五个倒位在该沙潜蝇簇的其他三个种中的存在情况。这些结果揭示了沙潜蝇簇的染色体系统发育,但仍有许多问题悬而未决。

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