蚕业科学
蠶業科學
잠업과학
ACTA SERICOLOGICA SINICA
2010年
1期
157-164
,共8页
姜振%蔡明文%徐世清%房丽秀%司马杨虎
薑振%蔡明文%徐世清%房麗秀%司馬楊虎
강진%채명문%서세청%방려수%사마양호
家蚕实用品种%DNA多态性%随机扩增多态性DNA%简单重复序列
傢蠶實用品種%DNA多態性%隨機擴增多態性DNA%簡單重複序列
가잠실용품충%DNA다태성%수궤확증다태성DNA%간단중복서렬
Silkworm commercial variety%DNA polymorphism%Random amplified polymorphic DNA%Simple sequence repeat
分子标记是生物系统进化和亲缘关系分析的重要手段.利用RAPD和SSR标记对12个家蚕实用品种的基因组DNA进行多态性分析和聚类分析.采用21条RAPD引物对12个品种的基因组DNA扩增产生的清晰稳定条带数为196条,其中多态性片段143条,多态位点比例72.96%,品种间的遗传距离在0.157~0.352之间.采用32条SSR引物对12个品种的基因组DNA扩增产生的片段数为86条,其中多态性带80条,多态性位点比例93.02%,遗传距离在0.214~0.600之间.对12个家蚕品种的2种分子标记的单独聚类结果表现出一定差异,但均把12个品种分为中系、日系两大类,其中7532和湘晖、871和57B的亲缘关系较近,而传统分类于中系品种东34却聚类于日系,但又独立于其余6个日系品种.结合RAPD标记和SSR标记的12个品种间的遗传距离与聚类结果,更能准确地从分子水平上反映品种间的亲缘关系及其来源,是家蚕杂交育种亲本选择的依据.
分子標記是生物繫統進化和親緣關繫分析的重要手段.利用RAPD和SSR標記對12箇傢蠶實用品種的基因組DNA進行多態性分析和聚類分析.採用21條RAPD引物對12箇品種的基因組DNA擴增產生的清晰穩定條帶數為196條,其中多態性片段143條,多態位點比例72.96%,品種間的遺傳距離在0.157~0.352之間.採用32條SSR引物對12箇品種的基因組DNA擴增產生的片段數為86條,其中多態性帶80條,多態性位點比例93.02%,遺傳距離在0.214~0.600之間.對12箇傢蠶品種的2種分子標記的單獨聚類結果錶現齣一定差異,但均把12箇品種分為中繫、日繫兩大類,其中7532和湘暉、871和57B的親緣關繫較近,而傳統分類于中繫品種東34卻聚類于日繫,但又獨立于其餘6箇日繫品種.結閤RAPD標記和SSR標記的12箇品種間的遺傳距離與聚類結果,更能準確地從分子水平上反映品種間的親緣關繫及其來源,是傢蠶雜交育種親本選擇的依據.
분자표기시생물계통진화화친연관계분석적중요수단.이용RAPD화SSR표기대12개가잠실용품충적기인조DNA진행다태성분석화취류분석.채용21조RAPD인물대12개품충적기인조DNA확증산생적청석은정조대수위196조,기중다태성편단143조,다태위점비례72.96%,품충간적유전거리재0.157~0.352지간.채용32조SSR인물대12개품충적기인조DNA확증산생적편단수위86조,기중다태성대80조,다태성위점비례93.02%,유전거리재0.214~0.600지간.대12개가잠품충적2충분자표기적단독취류결과표현출일정차이,단균파12개품충분위중계、일계량대류,기중7532화상휘、871화57B적친연관계교근,이전통분류우중계품충동34각취류우일계,단우독립우기여6개일계품충.결합RAPD표기화SSR표기적12개품충간적유전거리여취류결과,경능준학지종분자수평상반영품충간적친연관계급기래원,시가잠잡교육충친본선택적의거.
Molecular marker technique is an important method in studying phylogenetic evolution and genetic relationship of organisms. The DNA polymorphism of 12 commercial silkworm varieties was analyzed based on RAPD and SSR molecular markers. Subsequently, cluster analysis was conducted. By using 21 RAPD primers to amplify the genomic DNAs of 12 silkworm varieties, 196 clearly distinguishable bands were obtained, among which 143 bands showed polymorphism, showing a polymorphism percentage of 72.96% and relative genetic distances ranging from 0.157 to 0.352 between different varieties. By using 32 SSR primers to amplify the genomic DNAs of 12 silkworm varieties, 86 distinguishable bands were obtained, among which 80 bands showed polymorphism, showing a polymorphism percentage of 93.02% and relative genetic distances ranging from 0.214 to 0.600 between different varieties. Although cluster analyses based on RAPD and SSR molecular markers of the 12 silkworm species yielded different results, both results classified the 12 silkworm varieties into Chinese strain and Japanese strain, among which the genetic relationship between strains 7532 and Xianghui and between strains 871 and 57B were relatively closer. However, Dong 34, a variety that belongs to Chinese strain in the traditional classification, was classified into Japanese strain, though it was independent of other 6 varieties from Japanese strain. The genetic distances and cluster results of the 12 varieties based on RAPD and SSR molecular markers could reflect genetic relationship and origin of different varieties at the molecular level more accurately, being important references for parent selection in silkworm cross breeding.