Feng Jiuhuan, Vick Brady A, Lee Mi-Kyung, Zhang Hong-Bin, Jan C C
Department of Plant Sciences, North Dakota State University, Fargo, ND 58105, USA.
Theor Appl Genet. 2006 Jun;113(1):23-32. doi: 10.1007/s00122-006-0265-7. Epub 2006 Apr 13.
Complementary BAC and BIBAC libraries were constructed from nuclear DNA of sunflower cultivar HA 89. The BAC library, constructed with BamHI in the pECBAC1 vector, contains 107,136 clones and has an average insert size of 140 kb. The BIBAC library was constructed with HindIII in the plant-transformation-competent binary vector pCLD04541 and contains 84,864 clones, with an average insert size of 137 kb. The two libraries combined contain 192,000 clones and are equivalent to approximately 8.9 haploid genomes of sunflower (3,000 Mb/1C), and provide a greater than 99% probability of obtaining a clone of interest. The frequencies of BAC and BIBAC clones carrying chloroplast or mitochondrial DNA sequences were estimated to be 2.35 and 0.04%, respectively, and insert-empty clones were less than 0.5%. To facilitate chromosome engineering and anchor the sunflower genetic map to its chromosomes, one to three single- or low-copy RFLP markers from each linkage group of sunflower were used to design pairs of overlapping oligonucleotides (overgos). Thirty-six overgos were designed and pooled as probes to screen a subset (5.1x) of the BAC and BIBAC libraries. Of the 36 overgos, 33 (92%) gave at least one positive clone and 3 (8%) failed to hit any clone. As a result, 195 BAC and BIBAC clones representing 19 linkage groups were identified, including 76 BAC clones and 119 BIBAC clones, further verifying the genome coverage and utility of the libraries. These BAC and BIBAC libraries and linkage group-specific clones provide resources essential for comprehensive research of the sunflower genome.
从向日葵品种HA 89的核DNA构建了互补的BAC文库和BIBAC文库。用BamHI在pECBAC1载体中构建的BAC文库包含107,136个克隆,平均插入片段大小为140 kb。BIBAC文库用HindIII在植物转化能力二元载体pCLD04541中构建,包含84,864个克隆,平均插入片段大小为137 kb。两个文库合起来包含192,000个克隆,相当于约8.9个向日葵单倍体基因组(3,000 Mb/1C),获得感兴趣克隆有大于99%的概率。携带叶绿体或线粒体DNA序列的BAC和BIBAC克隆的频率估计分别为2.35%和0.04%,插入空载体的克隆小于0.5%。为便于染色体工程并将向日葵遗传图谱锚定到其染色体上,从向日葵每个连锁群中选取一到三个单拷贝或低拷贝RFLP标记来设计重叠寡核苷酸对(重叠群)。设计了36个重叠群并合并作为探针来筛选BAC和BIBAC文库的一个子集(5.1倍)。在36个重叠群中,33个(92%)至少得到一个阳性克隆,3个(8%)未命中任何克隆。结果,鉴定出代表19个连锁群的195个BAC和BIBAC克隆,包括76个BAC克隆和119个BIBAC克隆,进一步验证了文库的基因组覆盖范围和实用性。这些BAC和BIBAC文库以及连锁群特异性克隆为向日葵基因组的全面研究提供了必不可少的资源。