生物
基因组
遗传学
重组酶
基因组进化
染色体
计算生物学
全基因组测序
进化生物学
基因
重组
作者
Yue Shen,Giovanni Stracquadanio,Yun Wang,Kun Yang,Leslie A. Mitchell,Yaxin Xue,Yizhi Cai,Tai Chen,Jessica S. Dymond,Kang Kang,Jianhui Gong,Xiaofan Zeng,Yongfen Zhang,Yingrui Li,Qiang Feng,Xun Xu,Jun Wang,Jian Wang,Huanming Yang,Jef D. Boeke
出处
期刊:Genome Research
[Cold Spring Harbor Laboratory Press]
日期:2015-11-13
卷期号:26 (1): 36-49
被引量:159
标识
DOI:10.1101/gr.193433.115
摘要
Synthetic chromosome rearrangement and modification by loxP -mediated evolution (SCRaMbLE) generates combinatorial genomic diversity through rearrangements at designed recombinase sites. We applied SCRaMbLE to yeast synthetic chromosome arm synIXR (43 recombinase sites) and then used a computational pipeline to infer or unscramble the sequence of recombinations that created the observed genomes. Deep sequencing of 64 synIXR SCRaMbLE strains revealed 156 deletions, 89 inversions, 94 duplications, and 55 additional complex rearrangements; several duplications are consistent with a double rolling circle mechanism. Every SCRaMbLE strain was unique, validating the capability of SCRaMbLE to explore a diverse space of genomes. Rearrangements occurred exclusively at designed loxPsym sites, with no significant evidence for ectopic rearrangements or mutations involving synthetic regions, the 99% nonsynthetic nuclear genome, or the mitochondrial genome. Deletion frequencies identified genes required for viability or fast growth. Replacement of 3′ UTR by non-UTR sequence had surprisingly little effect on fitness. SCRaMbLE generates genome diversity in designated regions, reveals fitness constraints, and should scale to simultaneous evolution of multiple synthetic chromosomes.
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