海洋科学
海洋科學
해양과학
MARINE SCIENCES
2009年
12期
4-8
,共5页
李宏俊%刘晓%杜雪地%宋蕊%张国范%胡景杰%包振民
李宏俊%劉曉%杜雪地%宋蕊%張國範%鬍景傑%包振民
리굉준%류효%두설지%송예%장국범%호경걸%포진민
海湾扇贝(Argopecten irradians)%微卫星%富集文库%无效等位基因%分离方式
海灣扇貝(Argopecten irradians)%微衛星%富集文庫%無效等位基因%分離方式
해만선패(Argopecten irradians)%미위성%부집문고%무효등위기인%분리방식
Bay scallop (Argopecten irradians)%SSR%microsatellite-enriched library%null allele%allele transmission
利用尼龙膜吸附杂交法构建了海湾扇贝的(AC)_(15)、(AG)_(15)微卫星富集文库,随机挑取3 000个克隆,经菌落原位杂交二次筛选共获得阳性克隆1 268个(42.3%).经序列测定和生物信息学分析后得到521个独立的阳性克隆,其中微卫星506个,小卫星15个.微卫星中,完美型248个,占总数的49.0%;非完美型216个,占42.7%;复合型42个,占8.3%;其中AG/TC重复占70.4%(356个),AC/TG重复29.6%(150个).选择其中的55条序列设计引物,筛选出其中的20对引物检测它们在海湾扇贝CC10家系的双亲和94个子代个体中的分离情况,结果表明:(1) 其中6个位点在母本和子代中发生分离,10个位点在父本和子代中发生分离,4个为双亲共享位点;(2) 2个位点存在无效等位基因;(3) 16个位点符合孟德尔遗传定律,4个位点的子代个体基因型频率偏离孟德尔遗传定律.上述结果表明,这些微卫星引物可以用于构建海湾扇贝的遗传连锁图谱,并且所构建的富集文库适用于微卫星标记的大规模开发.
利用尼龍膜吸附雜交法構建瞭海灣扇貝的(AC)_(15)、(AG)_(15)微衛星富集文庫,隨機挑取3 000箇剋隆,經菌落原位雜交二次篩選共穫得暘性剋隆1 268箇(42.3%).經序列測定和生物信息學分析後得到521箇獨立的暘性剋隆,其中微衛星506箇,小衛星15箇.微衛星中,完美型248箇,佔總數的49.0%;非完美型216箇,佔42.7%;複閤型42箇,佔8.3%;其中AG/TC重複佔70.4%(356箇),AC/TG重複29.6%(150箇).選擇其中的55條序列設計引物,篩選齣其中的20對引物檢測它們在海灣扇貝CC10傢繫的雙親和94箇子代箇體中的分離情況,結果錶明:(1) 其中6箇位點在母本和子代中髮生分離,10箇位點在父本和子代中髮生分離,4箇為雙親共享位點;(2) 2箇位點存在無效等位基因;(3) 16箇位點符閤孟德爾遺傳定律,4箇位點的子代箇體基因型頻率偏離孟德爾遺傳定律.上述結果錶明,這些微衛星引物可以用于構建海灣扇貝的遺傳連鎖圖譜,併且所構建的富集文庫適用于微衛星標記的大規模開髮.
이용니룡막흡부잡교법구건료해만선패적(AC)_(15)、(AG)_(15)미위성부집문고,수궤도취3 000개극륭,경균락원위잡교이차사선공획득양성극륭1 268개(42.3%).경서렬측정화생물신식학분석후득도521개독립적양성극륭,기중미위성506개,소위성15개.미위성중,완미형248개,점총수적49.0%;비완미형216개,점42.7%;복합형42개,점8.3%;기중AG/TC중복점70.4%(356개),AC/TG중복29.6%(150개).선택기중적55조서렬설계인물,사선출기중적20대인물검측타문재해만선패CC10가계적쌍친화94개자대개체중적분리정황,결과표명:(1) 기중6개위점재모본화자대중발생분리,10개위점재부본화자대중발생분리,4개위쌍친공향위점;(2) 2개위점존재무효등위기인;(3) 16개위점부합맹덕이유전정률,4개위점적자대개체기인형빈솔편리맹덕이유전정률.상술결과표명,저사미위성인물가이용우구건해만선패적유전련쇄도보,병차소구건적부집문고괄용우미위성표기적대규모개발.
Three genomic libraries enriched for (AC)_(15) and (AG)_(15) were constructed using the method of nylon membrane hybridization in bay scallop (Argopecten irradians). A total of 3 000 clones derived from the enrichment libraries were screened by (AC)_(15) and (AG)_(15) probes, and 1 268 (42.3%) were proved to contain microsatellite repeat sequences. One thousand positive clones were sequenced, 506 independent microsatellites, and 15 minisatellite sequences were obtained. Among the 506 microsatellite repeat sequences, 248 (49.0%) were identified to be perfect microsatellites, 216 imperfect(42.7%) and 42 compound (8.3%). Fifty-five primer pairs were designed and amplified in one bay scallop family to test their polymorphism in this family. Twenty polymorphic microsatellite markers were selected to analyze their segregation and inheritance in parents and their 94 progenies of this bay scallop family, among which 4 were polymorphic in both parents, 6 in female and 10 in male. Two markers were observed to produce null alleles; and when null alleles were considered, there were 4 loci showing segregation distortion at 5% significance level. These results indicated that the microsatellite-enriched libraries constructed in the present study are efficient and suitable to isolate a large amount of microsatellite markers in bay scallop.