TY - JOUR
T1 - Targeted introgression of a wheat stem rust resistance gene by DNA marker-assisted chromosome engineering
AU - Niu, Zhixia
AU - Klindworth, Daryl L.
AU - Friesen, Timothy L.
AU - Chao, Shiaoman
AU - Jin, Yue
AU - Cai, Xiwen
AU - Xu, Steven S.
PY - 2011/4
Y1 - 2011/4
N2 - Chromosome engineering is a useful strategy for transfer of alien genes from wild relatives into modern crops. However, this strategy has not been extensively used for alien gene introgression in most crops due to low efficiency of conventional cytogenetic techniques. Here, we report an improved scheme of chromosome engineering for efficient elimination of a large amount of goat grass (Aegilops speltoides) chromatin surrounding Sr39, a gene that provides resistance to multiple stem rust races, including Ug99 (TTKSK) in wheat. The wheat ph1b mutation, which promotes meiotic pairing between homoeologous chromosomes, was employed to induce recombination between wheat chromosome 2B and goatgrass 2S chromatin using a backcross scheme favorable for inducing and detecting the homoeologous recombinants with small goat grass chromosome segments. Forty recombinants with Sr39 with reduced surrounding goat grass chromatin were quickly identified from 1048 backcross progenies through disease screening and molecular marker analysis. Four of the recombinants carrying Sr39 with a minimal amount of goatgrass chromatin (2.87-9.15% of the translocated chromosomes) were verified using genomic in situ hybridization. Approximately 97% of the goat grass chromatin was eliminated in one of the recombinants, in which a tiny goat grass chromosome segment containing Sr39 was retained in the wheat genome. Localization of the goat grass chromatin in the recombinants led to rapid development of three molecular markers tightly linked to Sr39. The new wheat lines and markers provide useful resources for the ongoing global effort to combat Ug99. This study has demonstrated great potential of chromosome engineering in genome manipulation for plant improvement.
AB - Chromosome engineering is a useful strategy for transfer of alien genes from wild relatives into modern crops. However, this strategy has not been extensively used for alien gene introgression in most crops due to low efficiency of conventional cytogenetic techniques. Here, we report an improved scheme of chromosome engineering for efficient elimination of a large amount of goat grass (Aegilops speltoides) chromatin surrounding Sr39, a gene that provides resistance to multiple stem rust races, including Ug99 (TTKSK) in wheat. The wheat ph1b mutation, which promotes meiotic pairing between homoeologous chromosomes, was employed to induce recombination between wheat chromosome 2B and goatgrass 2S chromatin using a backcross scheme favorable for inducing and detecting the homoeologous recombinants with small goat grass chromosome segments. Forty recombinants with Sr39 with reduced surrounding goat grass chromatin were quickly identified from 1048 backcross progenies through disease screening and molecular marker analysis. Four of the recombinants carrying Sr39 with a minimal amount of goatgrass chromatin (2.87-9.15% of the translocated chromosomes) were verified using genomic in situ hybridization. Approximately 97% of the goat grass chromatin was eliminated in one of the recombinants, in which a tiny goat grass chromosome segment containing Sr39 was retained in the wheat genome. Localization of the goat grass chromatin in the recombinants led to rapid development of three molecular markers tightly linked to Sr39. The new wheat lines and markers provide useful resources for the ongoing global effort to combat Ug99. This study has demonstrated great potential of chromosome engineering in genome manipulation for plant improvement.
UR - http://www.scopus.com/inward/record.url?scp=79955374806&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79955374806&partnerID=8YFLogxK
U2 - 10.1534/genetics.110.123588
DO - 10.1534/genetics.110.123588
M3 - Article
C2 - 21242535
AN - SCOPUS:79955374806
SN - 0016-6731
VL - 187
SP - 1011
EP - 1021
JO - Genetics
JF - Genetics
IS - 4
ER -