Miller Danny E, Cook Kevin R, Hemenway Elizabeth A, Fang Vivienne, Miller Angela L, Hales Karen G, Hawley R Scott
Stowers Institute for Medical Research, Kansas City, Missouri 64110.
MD-PhD Physician-Scientist Training Program and.
G3 (Bethesda). 2018 Mar 28;8(4):1161-1171. doi: 10.1534/g3.118.200021.
Balancer chromosomes are multiply inverted and rearranged chromosomes used in for many tasks, such as maintaining mutant alleles in stock and complex stock construction. Balancers were created before molecular characterization of their breakpoints was possible, so the precise locations of many of these breakpoints are unknown. Here, we report or confirm the positions of the 14 euchromatic breakpoints on the chromosome balancers , , , and This total includes three breakpoints involved in a complex rearrangement on that is associated with the duplication of two genomic regions. Unbiased sequencing of several balancers allowed us to identify stocks with incorrectly identified balancers as well as single and double crossover events that had occurred between chromosome balancers and their homologs. The confirmed crossover events that we recovered were at least 2 Mb from the closest inversion breakpoint, consistent with observations from other balancer chromosomes. Balancer chromosomes differ from one another both by large tracts of sequence diversity generated by recombination and by small differences, such as single nucleotide polymorphisms (SNPs). Therefore, we also report loss-of-function mutations carried by these chromosomes and unique SNP and InDel polymorphisms present on only single balancers. These findings provide valuable information about the structure of commonly used chromosome balancers and extend recent work examining the structure of and chromosome balancers. Finally, these observations provide new insights into how the sequences of individual balancers have diverged over time.
平衡染色体是经过多次倒位和重排的染色体,可用于许多任务,例如在品系中维持突变等位基因以及构建复杂品系。平衡染色体是在其断点的分子特征得以确定之前创建的,因此许多这些断点的确切位置尚不清楚。在这里,我们报告或确认了染色体平衡体、、和上14个常染色质断点的位置。这一总数包括与两个基因组区域重复相关的复杂重排中涉及的三个断点。对几个平衡体进行无偏差测序使我们能够识别平衡体鉴定错误的品系,以及染色体平衡体与其同源染色体之间发生的单交换和双交换事件。我们检测到的已确认交换事件距离最近的倒位断点至少2 Mb,这与其他平衡染色体的观察结果一致。平衡染色体彼此之间的差异,既体现在由重组产生的大片段序列多样性上,也体现在小差异上,如单核苷酸多态性(SNP)。因此,我们还报告了这些染色体携带的功能丧失突变以及仅存在于单个平衡体上的独特SNP和插入缺失多态性。这些发现为常用染色体平衡体的结构提供了有价值的信息,并扩展了最近对和染色体平衡体结构的研究工作。最后,这些观察结果为单个平衡体的序列如何随时间发生分化提供了新的见解。