Institute for Systems Biology, Seattle, Washington, USA.
Nat Methods. 2013 Jul;10(7):671-5. doi: 10.1038/nmeth.2479. Epub 2013 May 12.
Tetrad analysis has been a gold-standard genetic technique for several decades. Unfortunately, the need to manually isolate, disrupt and space tetrads has relegated its application to small-scale studies and limited its integration with high-throughput DNA sequencing technologies. We have developed a rapid, high-throughput method, called barcode-enabled sequencing of tetrads (BEST), that uses (i) a meiosis-specific GFP fusion protein to isolate tetrads by FACS and (ii) molecular barcodes that are read during genotyping to identify spores derived from the same tetrad. Maintaining tetrad information allows accurate inference of missing genetic markers and full genotypes of missing (and presumably nonviable) individuals. An individual researcher was able to isolate over 3,000 yeast tetrads in 3 h, an output equivalent to that of almost 1 month of manual dissection. BEST is transferable to other microorganisms for which meiotic mapping is significantly more laborious.
四联体分析几十年来一直是一种黄金标准的遗传技术。不幸的是,需要手动分离、破坏和间隔四联体,这将其应用限制在小规模研究中,并限制了其与高通量 DNA 测序技术的整合。我们开发了一种快速、高通量的方法,称为带有条形码的四联体测序(BEST),该方法使用 (i) 一种减数分裂特异性 GFP 融合蛋白通过 FACS 分离四联体,和 (ii) 在基因分型过程中读取的分子条形码,以识别来自同一四联体的孢子。保持四联体信息可以准确推断缺失的遗传标记和缺失(大概是不可存活的)个体的完整基因型。单个研究人员能够在 3 小时内分离出 3000 多个酵母四联体,其产量相当于近 1 个月的手动解剖。BEST 可转移到其他微生物,对于这些微生物来说,减数分裂图谱绘制要困难得多。