作物学报
作物學報
작물학보
ACTA AGRONOMICA SINICA
2006年
4期
515-521
,共7页
陈静%江玲%王春明%池桥宏%翟虎渠%万建民
陳靜%江玲%王春明%池橋宏%翟虎渠%萬建民
진정%강령%왕춘명%지교굉%적호거%만건민
水稻%数量性状基因座(QTL)%分子标记%花粉不育%杂种不育性
水稻%數量性狀基因座(QTL)%分子標記%花粉不育%雜種不育性
수도%수량성상기인좌(QTL)%분자표기%화분불육%잡충불육성
Rice ( Oryza sativa L. )%Quantitative trait loci (QTL)%Molecular marker%Pollen sterility%Hybrid sterility
以IR36(indica)和热研2号(japonica,广亲和品种)为亲本,构建了包含180个单株的F2群体及包括110个标记的分子连锁图谱.利用该F2群体,进行了水稻花粉不育数量性状基因座(quantitative trait locus,QTL)的检测和遗传效应分析,共检测到3个花粉不育QTL,分别位于第3、5、7染色体上,此外,共检测到9个由雄配子引起的偏分离QTL,其中7个与ga-14和ga-11位点的配子败育类型相同.与花粉形态鉴定相比,偏分离的数据对检测F1杂种花粉败育基因更为敏感.在第5、6染色体上控制偏分离的2个QTL位点,其杂合基因型出现的频率偏高.在qHPS-5位点,粳型纯合子表现出比杂合子和籼型纯合子更低的育性水平.本研究获得的分子标记将有助于聚合尽可能多的中性亲和基因以解决亚种间F1杂种的花粉不育性问题.
以IR36(indica)和熱研2號(japonica,廣親和品種)為親本,構建瞭包含180箇單株的F2群體及包括110箇標記的分子連鎖圖譜.利用該F2群體,進行瞭水稻花粉不育數量性狀基因座(quantitative trait locus,QTL)的檢測和遺傳效應分析,共檢測到3箇花粉不育QTL,分彆位于第3、5、7染色體上,此外,共檢測到9箇由雄配子引起的偏分離QTL,其中7箇與ga-14和ga-11位點的配子敗育類型相同.與花粉形態鑒定相比,偏分離的數據對檢測F1雜種花粉敗育基因更為敏感.在第5、6染色體上控製偏分離的2箇QTL位點,其雜閤基因型齣現的頻率偏高.在qHPS-5位點,粳型純閤子錶現齣比雜閤子和秈型純閤子更低的育性水平.本研究穫得的分子標記將有助于聚閤儘可能多的中性親和基因以解決亞種間F1雜種的花粉不育性問題.
이IR36(indica)화열연2호(japonica,엄친화품충)위친본,구건료포함180개단주적F2군체급포괄110개표기적분자련쇄도보.이용해F2군체,진행료수도화분불육수량성상기인좌(quantitative trait locus,QTL)적검측화유전효응분석,공검측도3개화분불육QTL,분별위우제3、5、7염색체상,차외,공검측도9개유웅배자인기적편분리QTL,기중7개여ga-14화ga-11위점적배자패육류형상동.여화분형태감정상비,편분리적수거대검측F1잡충화분패육기인경위민감.재제5、6염색체상공제편분리적2개QTL위점,기잡합기인형출현적빈솔편고.재qHPS-5위점,갱형순합자표현출비잡합자화선형순합자경저적육성수평.본연구획득적분자표기장유조우취합진가능다적중성친화기인이해결아충간F1잡충적화분불육성문제.
To estimate QTL for the pollen sterility, an F2 population of 180 plants from an indica / japonica hybrid was tested with 110 molecular markers. By the genome wide screening, three QTLs were identified for the pollen sterility on chromosomes 3, 5, 7, respectively. In addition, a total of nine QTL for segregation distortion via male gametes were mapped on rice chromosomes, of which seven QTLs were suggested to be the same type of gamete abortion as found at ga14 and ga-11. The distortion data seemed to be more sensitive to detection of pollen abortion genes in the F1 hybrid than the morphological inspection of pollen. Two QTLs for the segregation distortion on chromosomes 5 and 6 indicated an abnormally high frequency of heterozygous genotype. At a locus indicated by qHPS-5, japonica-type homozygote showed a lower fertility level than the heterozygotes and indica-type homozygote. The molecular markers identified here would be useful in introducing a set of new and known sterility-neutral alleles to solve the pollen sterility problem in subspecific F1 hybrids. Further, the present results could be helpful to combine as many neutral alleles for distortion as possible on whole genome basis to stabilize the pollen fertility as a whole.