江苏农业学报
江囌農業學報
강소농업학보
JIANGSU JOURNAL OF AGRICULTURAL SCIENCES
2014年
3期
486-490
,共5页
翟国伟%王华%邹桂花%邵健丰%陶跃之
翟國偉%王華%鄒桂花%邵健豐%陶躍之
적국위%왕화%추계화%소건봉%도약지
高粱%芒%Awn3.1%SSR标记%基因定位
高粱%芒%Awn3.1%SSR標記%基因定位
고량%망%Awn3.1%SSR표기%기인정위
sorghum%awn%Awn3. 1%SSR marker%gene mapping
为了确定高粱有、无芒表型的遗传特性,以无芒高粱品种Btx623和有芒品种7361为亲本做杂交,分析了F1植株和F2分离群体中的1155个单株的芒性基因遗传规律,结果显示有芒性状是受1个隐性单基因Awn3.1控制的质量性状。利用覆盖高粱10条染色体的自行开发的250对SSR引物在两亲本间筛选多态性标记,利用这些标记和22个表型有芒的F2隐性单株对芒性基因进行初定位,将目标基因定位在第3号染色体SSR标记sm03100和sm03108之间,与两标记的遗传距离分别为11.4 cM和4.5 cM。为了进一步缩小定位区间,对亲本7361的相关区段进行了测序,与已公布的Btx623序列比对后设计了InDel标记,并把定位群体扩大到214个F2隐性单株。通过扩大群体和开发新的标记,将目的基因Awn3.1精细定位在标记InDel-1和InDel-2之间的约115 kb范围内。
為瞭確定高粱有、無芒錶型的遺傳特性,以無芒高粱品種Btx623和有芒品種7361為親本做雜交,分析瞭F1植株和F2分離群體中的1155箇單株的芒性基因遺傳規律,結果顯示有芒性狀是受1箇隱性單基因Awn3.1控製的質量性狀。利用覆蓋高粱10條染色體的自行開髮的250對SSR引物在兩親本間篩選多態性標記,利用這些標記和22箇錶型有芒的F2隱性單株對芒性基因進行初定位,將目標基因定位在第3號染色體SSR標記sm03100和sm03108之間,與兩標記的遺傳距離分彆為11.4 cM和4.5 cM。為瞭進一步縮小定位區間,對親本7361的相關區段進行瞭測序,與已公佈的Btx623序列比對後設計瞭InDel標記,併把定位群體擴大到214箇F2隱性單株。通過擴大群體和開髮新的標記,將目的基因Awn3.1精細定位在標記InDel-1和InDel-2之間的約115 kb範圍內。
위료학정고량유、무망표형적유전특성,이무망고량품충Btx623화유망품충7361위친본주잡교,분석료F1식주화F2분리군체중적1155개단주적망성기인유전규률,결과현시유망성상시수1개은성단기인Awn3.1공제적질량성상。이용복개고량10조염색체적자행개발적250대SSR인물재량친본간사선다태성표기,이용저사표기화22개표형유망적F2은성단주대망성기인진행초정위,장목표기인정위재제3호염색체SSR표기sm03100화sm03108지간,여량표기적유전거리분별위11.4 cM화4.5 cM。위료진일보축소정위구간,대친본7361적상관구단진행료측서,여이공포적Btx623서렬비대후설계료InDel표기,병파정위군체확대도214개F2은성단주。통과확대군체화개발신적표기,장목적기인Awn3.1정세정위재표기InDel-1화InDel-2지간적약115 kb범위내。
The inheritance character of the awnness of sorghum were investigated in F1 and 1 155 individuals of F2 segregation population derived from a cross between awnless cultivar Btx623 and awned cultivar 7361. It was showed that the trait of awnness was controlled by a single recessive gene. The polymorphism of totally 250 SSR markers distributed throughout the genome of sorghum were identified. The polymorphic markers and 22 recessive F2 plants were used to prima-rily map the gene. The gene was located between markers sm03100 and sm03108 on chromosome 3, with genetic distances of 11. 4 cM and 4. 5 cM, respectively. To narrow down the located interval, InDel markers were developed through sequen-cing 7361 and alignment with Btx623, and the mapping population was enlarged to 214 recessive F2 plants. With newly mined InDel markers and enlarged population, the target region harboring Awn3. 1 was finally narrowed down to a 115 kb fragment between markers InDel-1 and InDel-2.