广州大学学报:自然科学版
廣州大學學報:自然科學版
엄주대학학보:자연과학판
Journal og Guangzhou University:Natural Science Edition
2011年
4期
32-35
,共4页
田长恩%周玉萍%Hideki Muto%Kotaro T Yamamoto
田長恩%週玉萍%Hideki Muto%Kotaro T Yamamoto
전장은%주옥평%Hideki Muto%Kotaro T Yamamoto
生长素反应因子7%生长素反应因子8%arf8%nph4/arf7%长下胚轴表型
生長素反應因子7%生長素反應因子8%arf8%nph4/arf7%長下胚軸錶型
생장소반응인자7%생장소반응인자8%arf8%nph4/arf7%장하배축표형
Auxin Response Factor 7%Auxin Response Factor 8%arf8%nph4/arf7%long-hypocotyl phenotype
通过对拟南芥(Arabidopsis thaliana)ARF8和NPH4/ARF7基因的突变体以及有关双突变体的下胚轴长度的表型和遗传分析,探讨了arf8—1、nph4—102和nph4—107长下胚轴表型的起源.结果表明,ARF8基因的其他突变体arf8—2、arf8—3和arf8-4都没有表现出类似于。arf8-1的长下胚轴表型;在与ARF8同源性较高的NPH4/ARF7的突变体中,突变位点与arf8-J相似的nph4—102和nph4—107表现出与aoOd一,相似的长下胚轴表型和不完全显性的遗传方式;双突变体arf8-J nph4—102的下胚轴长度比两个单突变体的长,说明arf8-J与nph4—102在长下胚轴表型上存在加性效应.因此,arf8-J、nph4—102和nph4—107的长下胚轴表型极可能源于相应突变体蛋白的产生,而非相关基因功能的缺失.
通過對擬南芥(Arabidopsis thaliana)ARF8和NPH4/ARF7基因的突變體以及有關雙突變體的下胚軸長度的錶型和遺傳分析,探討瞭arf8—1、nph4—102和nph4—107長下胚軸錶型的起源.結果錶明,ARF8基因的其他突變體arf8—2、arf8—3和arf8-4都沒有錶現齣類似于。arf8-1的長下胚軸錶型;在與ARF8同源性較高的NPH4/ARF7的突變體中,突變位點與arf8-J相似的nph4—102和nph4—107錶現齣與aoOd一,相似的長下胚軸錶型和不完全顯性的遺傳方式;雙突變體arf8-J nph4—102的下胚軸長度比兩箇單突變體的長,說明arf8-J與nph4—102在長下胚軸錶型上存在加性效應.因此,arf8-J、nph4—102和nph4—107的長下胚軸錶型極可能源于相應突變體蛋白的產生,而非相關基因功能的缺失.
통과대의남개(Arabidopsis thaliana)ARF8화NPH4/ARF7기인적돌변체이급유관쌍돌변체적하배축장도적표형화유전분석,탐토료arf8—1、nph4—102화nph4—107장하배축표형적기원.결과표명,ARF8기인적기타돌변체arf8—2、arf8—3화arf8-4도몰유표현출유사우。arf8-1적장하배축표형;재여ARF8동원성교고적NPH4/ARF7적돌변체중,돌변위점여arf8-J상사적nph4—102화nph4—107표현출여aoOd일,상사적장하배축표형화불완전현성적유전방식;쌍돌변체arf8-J nph4—102적하배축장도비량개단돌변체적장,설명arf8-J여nph4—102재장하배축표형상존재가성효응.인차,arf8-J、nph4—102화nph4—107적장하배축표형겁가능원우상응돌변체단백적산생,이비상관기인공능적결실.
We previously reported that arf8-1, a semidominant T-DNA insertion line of ARF8 gene, showed a long-hypocotyl phenotype when grown in white light. However, no report mentioned the similar phenotype in other mutant lines of ARFS. Through phenotypic and genetic analyses on hypocityl length of different mutant lines of ARF8 and NPH4/ARF7 gene, origin of long-hypocotyl phenotype in arf8-1, nph4-102 and nph4-107 has been probed. Here we reported that arfd-2, arf8-3 and arf8-4 indeed display same hypocotyls length with corre- sponding wild type. Among mutant lines of NPH4/ARF7 gene, nph4-102 and nph4-107 showed long-hypocotyl phenotype, too. Also, F1 of Col crossing with nph4-102 and nph4-107 show middle length of hypocotyl between wild type and mutant, meaning that they are semidominant, too. Hypocotyl length of double mutant arf8-1 nph4-102 is longer than each single mutant, indicating the independent action between arf8-1 and nph4-102 in controlling elongation of hypocotyls. Genomic sequence analyses showed the mutation sites of arf8-1, nph4-102 and nph4-107 are at the top of DNA bind domain in ARF8 and NPH4/ARF7 and may give rise to similar truncate proteins including part of hypocotyl phenotype of aft'd-l, of ARF8 gene or NPH4/ARF7 DNA bind domain of related genes. nph4-102 and nph4-107 results from gene Therefore, it is most possible that the long the truncate proteins but not loss-of-function