福建农业学报
福建農業學報
복건농업학보
FUJIAN JOURNAL OF AGRICULTURAL SCIENCES
2014年
1期
40-46
,共7页
卢丽芳%朱海生%温庆放%林义章
盧麗芳%硃海生%溫慶放%林義章
로려방%주해생%온경방%림의장
南瓜%SRAP%分子标记%PCR扩增
南瓜%SRAP%分子標記%PCR擴增
남과%SRAP%분자표기%PCR확증
Squash%SRAP%molecular marker%PCR amplification
以‘密本’南瓜作为筛选体系的材料,通过单因素试验对南瓜20μL SRAP-PCR扩增体系的Mg2+、dNTP、 Taq酶、引物及DNA浓度和扩增程序的退火温度与循环次数进行优化,筛选出各组分的最佳浓度、最佳的退火温度和最佳循环次数。试验结果确立南瓜最佳的20μL SRAP体系为:0.2 mmol · L -1 dNTP ,1.5 U Taq酶,80 ng DNA ,0.16μmol·L -1的单条引物,Mg2+1.5 mmol·L -1,2μL 10×Buffer ;最佳扩增程序为:94℃预变性5min;94℃1 min ,35℃1 min ,72℃1 min ,5个循环;94℃1 min ,52℃1 min ,72℃1 min 35个循环;最后72℃延伸10 min。选用17个南瓜品种对确立扩增体系及扩增程序进行验证,检测结果表现为扩增产物条带清晰明亮、多态性丰富、特异性强、重复性好,表明本试验所确定的反应体系及反应程序适用于南瓜的SRAP分子标记。
以‘密本’南瓜作為篩選體繫的材料,通過單因素試驗對南瓜20μL SRAP-PCR擴增體繫的Mg2+、dNTP、 Taq酶、引物及DNA濃度和擴增程序的退火溫度與循環次數進行優化,篩選齣各組分的最佳濃度、最佳的退火溫度和最佳循環次數。試驗結果確立南瓜最佳的20μL SRAP體繫為:0.2 mmol · L -1 dNTP ,1.5 U Taq酶,80 ng DNA ,0.16μmol·L -1的單條引物,Mg2+1.5 mmol·L -1,2μL 10×Buffer ;最佳擴增程序為:94℃預變性5min;94℃1 min ,35℃1 min ,72℃1 min ,5箇循環;94℃1 min ,52℃1 min ,72℃1 min 35箇循環;最後72℃延伸10 min。選用17箇南瓜品種對確立擴增體繫及擴增程序進行驗證,檢測結果錶現為擴增產物條帶清晰明亮、多態性豐富、特異性彊、重複性好,錶明本試驗所確定的反應體繫及反應程序適用于南瓜的SRAP分子標記。
이‘밀본’남과작위사선체계적재료,통과단인소시험대남과20μL SRAP-PCR확증체계적Mg2+、dNTP、 Taq매、인물급DNA농도화확증정서적퇴화온도여순배차수진행우화,사선출각조분적최가농도、최가적퇴화온도화최가순배차수。시험결과학립남과최가적20μL SRAP체계위:0.2 mmol · L -1 dNTP ,1.5 U Taq매,80 ng DNA ,0.16μmol·L -1적단조인물,Mg2+1.5 mmol·L -1,2μL 10×Buffer ;최가확증정서위:94℃예변성5min;94℃1 min ,35℃1 min ,72℃1 min ,5개순배;94℃1 min ,52℃1 min ,72℃1 min 35개순배;최후72℃연신10 min。선용17개남과품충대학립확증체계급확증정서진행험증,검측결과표현위확증산물조대청석명량、다태성봉부、특이성강、중복성호,표명본시험소학정적반응체계급반응정서괄용우남과적SRAP분자표기。
In order to screen out the optimal concentrations of various components ,the best annealing temperature and the best cycle times ,we took an optimization experiment of 20 μL SRAP-PCR amplification system with single factor design which focused on the concentrated of Mg 2+ ,dNTP ,Taq DNA polymerase ,primer ,template DNA and the amplification procedures of annealing temperature and cycle times by using the Squash ‘Miben’ as the material of filter system .Experimental results showed the optimal 20 μL SRAP amplification of Squash contained 0.2 mmol · L -1 dNTP ,1.5 U Taq DNA polymerase ,80 ng template DNA ,0.16 μmol · L -1 single primer ,1.5 mmol · L -1 Mg2+ ,2 μL 10 × Buffer .And the best amplification procedure was pre-denaturation at 94℃ for 5 min . Next by 5 cycles of denaturation at 94℃for 1 min ,anneal at 35℃ for 1 min and the extension at 72℃ for 1min then 35 cycles of 94℃ for 1 min ,52℃ for 1 min and 72℃ for 1 min and a final extension at 72℃ for 10min . The amplification system and the amplification procedures were tested by using 17 variaties of Squash .The test results showed the amplification products which were clear and bright ,abundant polymorphism ,strong specificity and good repeatability .Accordingly ,it was suitable for SRAP analysis of Squash .