همسانه سازی بخشی از ژن کدکننده آنزیم کیتیناز کلاس 3 از گیاه کدو حلوایی
پذیرفته شده برای پوستر
عنوان دوره: سیزدهمین کنگره زراعت و اصلاح نباتات ایران
نویسندگان
1داﻧﺸﺠﻮی ﻛﺎرﺷﻨﺎﺳﻲ ارﺷﺪ ﺑﻴﻮﺗﻜﻨﻮﻟﻮژی داﻧﺸﮕﺎه ﭘﻴﺎم ﻧﻮر واﺣﺪ ﻛﺮج
2اﺳﺘﺎدﻳﺎر ﭘﮋوﻫﺸﻜﺪه ژﻧﺘﻴﻚ و زﻳﺴﺖ ﻓﻨﺎوری ﻛﺸﺎورزی ﻃﺒﺮﺳﺘﺎن ، داﻧﺸﮕﺎه ﻋﻠﻮم ﻛﺸﺎورزی و ﻣﻨﺎﺑﻊ ﻃﺒﻴﻌﻲ ﺳﺎری
3اﺳﺘﺎدﻳﺎر داﻧﺸﮕﺎه ﭘﻴﺎم ﻧﻮر واﺣﺪ ﻛﺮج
چکیده
آﻧﺰﻳﻢﻫﺎی ﻛﻴﺘﻴﻨﺎز ﻧﻮﻋﻲ ﮔﻠﻴﻜﻮزﻳﻞ ﻫﻴﺪروﻻز ﺑﺎ ﻗﺪرت ﻛﺎﺗﺎﻟﻴﺰ ﻣﻲﺑﺎﺷﻨﺪ ﻛﻪ ﻗﺎدرﻧﺪ ﭘﻴﻮﻧﺪ ﮔﻠﻴﻜﻮزﻳﺪا β-1,4 را در ﺑﻴﻦ واﺣﺪﻫﺎی-N اﺳﺘﻴﻞ- ﮔﻠﻮﻛﺰآﻣﻴﻦ )GlcNAc( ﺑﺸﻜﻨﻨﺪ.اﻳﻦ آﻧﺰﻳﻢﻫﺎ از ﻣﻬﻤﺘﺮﻳﻦ ﺣﺎﻧﻮادهﻫﺎی ﭘﺮوﺗﺌﻴﻨﻲ دﺧﻴﻞ در ﻣﻘﺎوﻣﺖ ﺑﻪ ﺑﻴﻤﺎریﻫﺎی ﻗﺎرﭼﻲ در ﮔﻴﺎﻫﺎن ﻣﻲﺑﺎﺷﻨﺪ. ﺧﺎﻧﻮاده ﻛﺪوﻳﻴﺎن، ﺧﺎﻧﻮاده ﺑﺰرﮔﻲ ﺑﻮده ﻛﻪ ﺷﺎﻣﻞ ﺗﻌﺪاد زﻳﺎدی ﮔﻮﻧﻪﻫﺎی وﺣﺸﻲ و زراﻋﻲ ﻣﻲﺑﺎﺷﺪ، ﮔﻮﻧﻪﻫﺎﻳﻲ ﺑﺎ ﻣﻘﺎوﻣﺖ ﺑﺎﻻ ﺑﻪ ﺑﻴﻤﺎریﻫﺎی ﻗﺎرﭼﻲ ﻛﻪ ﻣﻲﺗﻮاﻧﻨﺪ ﺑﻪ ﻋﻨﻮان ﻣﻨﺎﺑﻊ ژﻧﺘﻴﻜﻲ ﻣﻘﺎوﻣﺖ ﺑﺮای اﻧﺘﻘﺎل ژن و اﺻﻼح ارﻗﺎم ﺣﺴﺎس زارﻋﻲ ﻣﻮرد اﺳﺘﻔﺎده ﻗﺮار ﮔﻴﺮﻧﺪ. در اﻳﻦ ﺗﺤﻘﻴﻖ ﺑﺎ اﺳﺘﻔﺎده از ﻫﻤﺮدﻳﻔﻲ ژن ﻛﻴﺘﻴﻨﺎز ﮔﻴﺎﻫﺎن ﺧﺎﻧﻮاده ﻛﺪوﺋﻴﺎن آﻏﺎزﮔﺮﻫﺎی دژﻧﺮه ﻃﺮاﺣﻲ ﺷﺪ،ﻣﺤﺼﻮل PCR ﭘﺲ از ﺧﺎﻟﺺ ﺳﺎزی در در وﻛﺘﻮر pTZ57R/Z ﻫﻤﺴﺎﻧﻪ ﺳﺎزی و ﺳﭙﺲ ﺗﻮاﻟﻲ ﻳﺎﺑﻲ ﺷﺪ. ﻧﺘﺎﻳﺞ ﺣﻀﻮر ژن ﻛﻴﺘﻴﻨﺎز ﻛﻼس 3 را در ﮔﻴﺎﻫﺎن ﺧﺎﻧﻮاده ﻛﺪوﺋﻴﺎن ﺗﺎﻳﻴﺪ ﻣﻲﻛﻨﺪ. ﺑﺮرﺳﻲ داﻣﻨﻪ ﻫﺎی ژﻧﻲ و ﻣﻘﺎﻳﺴﻪ آن ﺑﺎ دادهﻫﺎی ﭘﺎﻳﮕﺎهﻫﺎی ﻧﻮﻛﻠﺌﻮﺗﻴﺪی و ﭘﺮوﺗﺌﻴﻨﻲ ﻧﺸﺎن داد اﻳﻦ ﻛﻴﺘﻴﻨﺎز ﺑﻪ ﮔﺮوه ﻛﻴﺘﻴﻨﺎزﻫﺎی ﻛﻼس3 ﻛﻪ از ﻧﻮع اﺳﻴﺪی ﻫﺴﺘﻨﺪ ﺗﻌﻠﻖ دارد.
کلیدواژه ها
Title
Cloning the partial sequence of class III chitinase gene from Cucurbita moschata
Authors
Abstract
Chitinases act by hydrolytically cleaving the β-glycosidic linkages between GlcNAc. They are among the most important groups of pathogenesis related proteins conferring plants resistance to wide variety of fungal pathogens. These enzymes catalyze the hydrolysis of chitin, a linear homopolymer of β-1,4-linked N-acetylglucosamine residues. Among cultivated and wild cucurbits, some species have been proved to be resistant to certain fungal pathogens, which can be used as genetic resources for gene transfer and breeding of susceptible cultivated varieties. In this study degenerate primers were designed from other Cucurbitaceae family plants. Purified PCR product was cloned in pTZ57R/Z cloning vector and sequenced. The results determine the presence of class III chitinase in Cucurbita moschata using degenerate primers. Analysis of gene domains through seeking nucleotide and protein database indicated that the isolated sequence belong to class III chitinase which are commonly grouped as acidic chitinase.
Keywords
Cucurbitaceae, cloning, Chitinase