中国水产科学
中國水產科學
중국수산과학
Journal of Fishery Sciences of China
2014年
1期
197-202
,共6页
刘永新%刘海金%薛玲玲%王玉芬%张晓彦%司飞%孙朝徽%王桂兴
劉永新%劉海金%薛玲玲%王玉芬%張曉彥%司飛%孫朝徽%王桂興
류영신%류해금%설령령%왕옥분%장효언%사비%손조휘%왕계흥
牙鲆%有丝分裂%雌核发育%静水压%优化
牙鲆%有絲分裂%雌覈髮育%靜水壓%優化
아평%유사분렬%자핵발육%정수압%우화
Japanese flounder%mitosis%gynogenesis%hydrostatic pressure%optimization
本研究采用紫外线灭活的真鲷(Pagrus major)精子激活牙鲆(Paralichthys olivaceus)卵子,经过静水压机处理诱导有丝分裂雌核发育二倍体。优选施压起始时间、持续时间和压力大小3个方面参数,获得最佳参数组合为:起始时间60 min、持续时间6 min、施加压力650 kg/cm2。在此条件下的受精率最高为67.80%,孵化率54.23%,与其他处理组间达显著性差异(P<0.05)。用流式细胞仪检测未经静水压处理的胚胎,其 DNA 含量约为普通二倍体的1/2,即单倍体;检测有丝分裂雌核发育胚胎,其DNA含量与普通二倍体大体一致。结果表明,应用该方法可成功诱导获得牙鲆有丝分裂雌核发育二倍体。
本研究採用紫外線滅活的真鯛(Pagrus major)精子激活牙鲆(Paralichthys olivaceus)卵子,經過靜水壓機處理誘導有絲分裂雌覈髮育二倍體。優選施壓起始時間、持續時間和壓力大小3箇方麵參數,穫得最佳參數組閤為:起始時間60 min、持續時間6 min、施加壓力650 kg/cm2。在此條件下的受精率最高為67.80%,孵化率54.23%,與其他處理組間達顯著性差異(P<0.05)。用流式細胞儀檢測未經靜水壓處理的胚胎,其 DNA 含量約為普通二倍體的1/2,即單倍體;檢測有絲分裂雌覈髮育胚胎,其DNA含量與普通二倍體大體一緻。結果錶明,應用該方法可成功誘導穫得牙鲆有絲分裂雌覈髮育二倍體。
본연구채용자외선멸활적진조(Pagrus major)정자격활아평(Paralichthys olivaceus)란자,경과정수압궤처리유도유사분렬자핵발육이배체。우선시압기시시간、지속시간화압력대소3개방면삼수,획득최가삼수조합위:기시시간60 min、지속시간6 min、시가압력650 kg/cm2。재차조건하적수정솔최고위67.80%,부화솔54.23%,여기타처리조간체현저성차이(P<0.05)。용류식세포의검측미경정수압처리적배태,기 DNA 함량약위보통이배체적1/2,즉단배체;검측유사분렬자핵발육배태,기DNA함량여보통이배체대체일치。결과표명,응용해방법가성공유도획득아평유사분렬자핵발육이배체。
Mitotic gynogenetic diploid Japanese flounder, Paralichthys olivaceus were produced by activating eggs with UV irradiated sperm of red sea bream (Pagrus major), followed by hydrostatic pressure treatment to block the first mitotic division. The initiation time, duration time and pressure value of hydrostatic pressure were opti-mized in this study. The results showed that the treatment with hydrostatic pressure (650 kg/cm2) for 6 min starting 60 min after fertilization was the optimal parameters combination. Under this condition the fertilization rate and hatching rate at this scenario were 67.80%and 54.23%, respectively, which were significantly higher than that of all the other treatment groups(P<0.05). The embryo not treated by hydrostatic pressure (haploid) were identified via flow cytometer, and its relative DNA content was about half that of normal diploid. The mitotic gynogenetic embryo had the same DNA relative content with normal diploid. The analysis results showed that mitotic gynoge-netic diploids could be successfully prepared.