Deletion mapping of genetic regions associated with apomixis in Hieracium

被引:101
作者
Catanach, Andrew S.
Erasmuson, Sylvia K.
Podivinsky, Ellen
Jordan, Brian R.
Bicknell, Ross
机构
[1] New Zealand Inst Crop & Food Res Ltd, Christchurch 8140, New Zealand
[2] Lincoln Univ, Agr & Life Sci Div, Lincoln 7647, New Zealand
[3] Environm Sci & Res Ltd, Christchurch, New Zealand
关键词
amplified fragment length polymorphism (AFLP); meiosis; parthenogenesis; NON-MENDELIAN TRANSMISSION; PENNISETUM-SQUAMULATUM; RANUNCULUS-AURICOMUS; CHROMOSOMAL REGION; AGAMIC COMPLEXES; SEED DEVELOPMENT; GENOMIC REGION; APOSPORY; INHERITANCE; MARKERS;
D O I
10.1073/pnas.0605588103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although apomixis has been quoted as a technology with the potential to deliver benefits similar in scale to those achieved with the Green Revolution, very little is currently known of the genetic mechanisms that control this trait in plants. To address this issue, we developed Hieracium, a genus of daisies native to Eurasia and North America, as a genetic model to study apomixis. In a molecular mapping study, we defined the number of genetic loci involved in apomixis, and we explored dominance and linkage relationships between these loci. To avoid difficulties often encountered with inheritance studies of apomicts, we based our mapping effort on the use of deletion mutagenesis, coupled with amplified fragment length polymorphism (AFLP) as a genomic fingerprinting tool. The results indicate that apomixis in Hieracium caespitosum is controlled at two principal loci, one of which regulates events associated with the avoidance of meiosis (apomeiosis) and the other, an unlinked locus that controls events associated with the avoidance of fertilization (parthenogenesis). AFLP bands identified as central to both loci were isolated, sequenced, and used to develop sequence-characterized amplified region (SCAR) markers. The validity of the AFLP markers was verified by using a segregating population generated by hybridization. The validity of the SCAR markers was verified by their pattern of presence/absence in specific mutants. The mutants, markers, and genetic data derived from this work are now being used to isolate genes controlling apomixis in this system.
引用
收藏
页码:18650 / 18655
页数:6
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