CAJ | 학술논문

　　以西瓜品种8424和甜瓜品种甬甜3号作为接穗，以印度南瓜A（TLZ-B2-1-24，亲和）和印度南瓜B（Z079-1-2-17，不亲和）为砧木，配置瓜类异属间嫁接亲和/不亲和组合，利用SDS-PAGE技术，分析了瓜类异属间嫁接亲和组合（西瓜/印度南瓜A和甜瓜/印度南瓜A），以及嫁接不亲和组合（西瓜/印度南瓜B和甜瓜/印度南瓜B），在不同发育时期的全蛋白变化，分离分析了嫁接亲和/不亲和过程中产生的特异蛋白。结果表明：瓜类异属间嫁接亲和过程中，接穗（西瓜和甜瓜）组织蛋白和愈伤蛋白保持完整，砧木印度南瓜A的39 kDa愈伤特异蛋白在嫁接第10天后降解消失。瓜类异属间嫁接不亲和过程中，嫁接体的接穗部分出现了特异蛋白（西瓜36 kDa，甜瓜28 kDa）；砧木印度南瓜B在愈伤期间，自身组织严重降解，38 kDa的愈伤蛋白在嫁接体-印度南瓜B部分降解消失。这些由瓜类异属间嫁接亲和特性引起的接穗与砧木蛋白质谱带的变化结果，首次揭示了嫁接亲和特性在蛋白质水平上发生的作用机理。
　　이서과품충8424화첨과품충용첨3호작위접수，이인도남과A（TLZ-B2-1-24，친화）화인도남과B（Z079-1-2-17，불친화）위침목，배치과류이속간가접친화/불친화조합，이용SDS-PAGE기술，분석료과류이속간가접친화조합（서과/인도남과A화첨과/인도남과A），이급가접불친화조합（서과/인도남과B화첨과/인도남과B），재불동발육시기적전단백변화，분리분석료가접친화/불친화과정중산생적특이단백。결과표명：과류이속간가접친화과정중，접수（서과화첨과）조직단백화유상단백보지완정，침목인도남과A적39 kDa유상특이단백재가접제10천후강해소실。과류이속간가접불친화과정중，가접체적접수부분출현료특이단백（서과36 kDa，첨과28 kDa）；침목인도남과B재유상기간，자신조직엄중강해，38 kDa적유상단백재가접체-인도남과B부분강해소실。저사유과류이속간가접친화특성인기적접수여침목단백질보대적변화결과，수차게시료가접친화특성재단백질수평상발생적작용궤리。
The production of specific proteins during graft compatible /incompatible heterograft combination of cucurbitaceae was studied by SDS-PAGE electrophoresis.The seedlings of watermelon (Citrullus lanatus(Thunb.)) cultivar 8424 and melon(Cucumis melo L.) cultivar Yongtian No.3 were grafted onto the compatible rootstock of winter squash(Cucurbita maxima duch.ex lam) A(TLZ-B2-1-24) and incompatible rootstock winter squash B (Z079-1-2-17 ),to format the compatibility and incompatibility response of heterograft combination of watermelon /winter squash A and melon/winter squash A,and watermelon/winter squash B and melon/winter squash B,respec-tively.The results showed as the follows:a decrease in a 39 kDa callus protein band at the winter squash A stock of the compatible union was observed during the 10 days after grafting,and the culls proteins of scion(watermelon and melon) were still kept.During the incompatible heterograft stage ,two specific proteins(36 kDa for watermelon and 28 kDa for melon) were expressed in the scion,and the original protein of winter squash B were declined seriously and a 38 kDa callus protein were decreased.Those results presented here demonstrated the identification of the pro-teins related to graft compatibility/incompatibility response.These findings allow the assumption that molecular change mechanism takes place during graft formation in compatible /incompatible combinations for the first time .