生物学杂志
生物學雜誌
생물학잡지
JOURNAL OF BIOLOGY
2014年
5期
23-28
,共6页
李军%龚一富%胡朝阳%王何瑜
李軍%龔一富%鬍朝暘%王何瑜
리군%공일부%호조양%왕하유
紫色土豆%类黄酮3′,5′-羟化酶%花青素%基因表达
紫色土豆%類黃酮3′,5′-羥化酶%花青素%基因錶達
자색토두%류황동3′,5′-간화매%화청소%기인표체
Kye words purple potato%flavonoid 3′,5′-hydroxylase ( F3′5′H) gene%aanthocyanin%gene expression
类黄酮3′，5′羟-化酶（ flavonoid 3′，5′-hydroxylase， F3′5′H）是植物花青素生物合成途径中的一个关键酶，紫色土豆（ Solanum tueb or sum） F3′5′H基因的克隆将为花青素合成调控和花青素代谢工程研究提供优质基因资源。研究采用RACE技术克隆了紫色土豆F3′5′H基因的cDNA全长序列，用生物信息学方法对其核苷酸和蛋白质序列进行了分析，并用半定量PCR 技术分析了F3′5′H基因在不同组织中的表达情况，同时研究了赤霉素和蔗糖处理后F3′5′H基因表达与花青素积累之间的相关性。研究结果表明，克隆的紫色土豆F3′5′H的cDNA全长为1854 bp，包含一个1530 bp的完整ORF，共编码509个氨基酸。生物信息学分析表明，StF3′5′H基因推测编码的氨基酸序列与其它植物的F3′5′H蛋白的相似性很高。 StF3′5′H基因的表达具有组织特异性，在紫色土豆根、茎和叶柄中都有表达，其中在叶柄中表达最强，而在块茎、叶轴和叶片中几乎检测不到StF3′5′H基因的表达。赤霉素和蔗糖能促进紫色土豆StF3′5′H基因的表达，进而促进花青素的积累。
類黃酮3′，5′羥-化酶（ flavonoid 3′，5′-hydroxylase， F3′5′H）是植物花青素生物閤成途徑中的一箇關鍵酶，紫色土豆（ Solanum tueb or sum） F3′5′H基因的剋隆將為花青素閤成調控和花青素代謝工程研究提供優質基因資源。研究採用RACE技術剋隆瞭紫色土豆F3′5′H基因的cDNA全長序列，用生物信息學方法對其覈苷痠和蛋白質序列進行瞭分析，併用半定量PCR 技術分析瞭F3′5′H基因在不同組織中的錶達情況，同時研究瞭赤黴素和蔗糖處理後F3′5′H基因錶達與花青素積纍之間的相關性。研究結果錶明，剋隆的紫色土豆F3′5′H的cDNA全長為1854 bp，包含一箇1530 bp的完整ORF，共編碼509箇氨基痠。生物信息學分析錶明，StF3′5′H基因推測編碼的氨基痠序列與其它植物的F3′5′H蛋白的相似性很高。 StF3′5′H基因的錶達具有組織特異性，在紫色土豆根、莖和葉柄中都有錶達，其中在葉柄中錶達最彊，而在塊莖、葉軸和葉片中幾乎檢測不到StF3′5′H基因的錶達。赤黴素和蔗糖能促進紫色土豆StF3′5′H基因的錶達，進而促進花青素的積纍。
류황동3′，5′간-화매（ flavonoid 3′，5′-hydroxylase， F3′5′H）시식물화청소생물합성도경중적일개관건매，자색토두（ Solanum tueb or sum） F3′5′H기인적극륭장위화청소합성조공화화청소대사공정연구제공우질기인자원。연구채용RACE기술극륭료자색토두F3′5′H기인적cDNA전장서렬，용생물신식학방법대기핵감산화단백질서렬진행료분석，병용반정량PCR 기술분석료F3′5′H기인재불동조직중적표체정황，동시연구료적매소화자당처리후F3′5′H기인표체여화청소적루지간적상관성。연구결과표명，극륭적자색토두F3′5′H적cDNA전장위1854 bp，포함일개1530 bp적완정ORF，공편마509개안기산。생물신식학분석표명，StF3′5′H기인추측편마적안기산서렬여기타식물적F3′5′H단백적상사성흔고。 StF3′5′H기인적표체구유조직특이성，재자색토두근、경화협병중도유표체，기중재협병중표체최강，이재괴경、협축화협편중궤호검측불도StF3′5′H기인적표체。적매소화자당능촉진자색토두StF3′5′H기인적표체，진이촉진화청소적적루。
Flavonoid 3′, 5′-hydroxylase ( F3 ′5′H) was a key enzyme involved in plant anthocyanin biosynthesis pathway.The cloning and expression analysis of F3′5′H gene from purple potato would provide the high quality genetic resources for further researches on the anthocyanin biosynthesis regulation and metabolic engineering.The full-length cDNA sequence of F3′5′H was cloned from Solanum tu-berosum using RACE techniques, and bioinformatic method was used to study cDNA sequence and deductive amino acid sequence. Semi-quantitative PCR method was used to analyze the expression of the F3′5′H gene in different organs.The relationship between the anthocyanin accumulation and the expression of the F3′5′H gene after processed by GA3 and sucrose were also analyzed.The results re-vealed that the full-ength cDNA sequence of StF 3′5′H consisted of 1 854 bp with an intact open reading frame of 1530 bp, encoding a polypeptide of 509 amino acids.Homology analysis indicated that the putative F3′5′H amino acid was highly homologous to other F3′5′H proteins from different species. StF3′5′H was expressed at different levels in different organs, which was found to be expressed in roots, stems and leafstalks ,but not in tubers, rachises or leaves .The highest expression level was detected in leafstalks.The anthocy-anin accumulation was induced by GA3 and sucrose, as well as the expression of StF 3′5′H.
