Study of the AtMAPR3 expression induced by d-amino levulinic acid and stresses in Arabidopsis

碩士 === 國立臺灣大學 === 生化科技學系 === 100 === Four functional-unknown proteins, AtMAPR2, AtMAPR3, AtMAPR4 and AtMAPR5, possessing sequence 30-40% similarity to MAPR (membrane associated progesterone receptor) are studied in this group. The cytochrome b5 like heme/steroid binding domain are highly conserved i...

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Main Authors: Shih-Yu Kuo, 郭時鈺
Other Authors: Chien-Chih Yang
Format: Others
Language:zh-TW
Published: 2012
Online Access:http://ndltd.ncl.edu.tw/handle/2wz367
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spelling ndltd-TW-100NTU051060062019-05-15T20:52:16Z http://ndltd.ncl.edu.tw/handle/2wz367 Study of the AtMAPR3 expression induced by d-amino levulinic acid and stresses in Arabidopsis 阿拉伯芥中 AtMAPR3 表現受 d-amino levulinic acid 及逆境誘導之研究 Shih-Yu Kuo 郭時鈺 碩士 國立臺灣大學 生化科技學系 100 Four functional-unknown proteins, AtMAPR2, AtMAPR3, AtMAPR4 and AtMAPR5, possessing sequence 30-40% similarity to MAPR (membrane associated progesterone receptor) are studied in this group. The cytochrome b5 like heme/steroid binding domain are highly conserved in these proteins, and they bind progesterone and heme in animals. The UV-visible absorption spectra showed AtMAPRs are hemoproteins. (Kao, 2010, unpublished) To study the physiological role of heme-binding ability of AtMAPR3, we analyzed whether or not the expression of AtMAPR3 are subjected to the heme concentration. In this study, 10-day-old seedlings were treated with a precursor of heme, δ-aminolevulinic acid (ALA). The results showed AtMAPR3 expression was three-fold-increased by ALA treatment under 16 h light / 8 h dark, and two-fold-increased under 24 h dark; however, when adding dipyridyl (DPD), the inhibitor of Fe-chelatase, the induction was blocked. The expression of AtMAPR3 was also induced by H2O2 and tert-butyl hydroxide (tBHP) about six-fold. H2O2 could be used as a second messenger to express the defence-related genes by jasmonic acid (JA), and JA increased AtMAPR3 expression about four-fold. To further study the physiology roles of AtMAPR3, we need to analyze the phenotype of AtMAPR3-KO and other mutants. In this study, AtMAPR3-KO, AtMAPR3-OX and WT were treated with H2O2, tBHP and methyl viologen (MeV), and the survival rate of AtMAPR3-KO was lower than WT slightly. However, AtMAPR3-OX showed no differences with WT. The results revealed that the downstream products of ALA, such as Mg-protoporphyrin IX or heme, could be a signal molecule which involved in the expression of AtMAPR3. The expression of AtMAPR3 in response to ROS needs to be further investigated in physiological aspect. Chien-Chih Yang 楊健志 2012 學位論文 ; thesis 102 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 國立臺灣大學 === 生化科技學系 === 100 === Four functional-unknown proteins, AtMAPR2, AtMAPR3, AtMAPR4 and AtMAPR5, possessing sequence 30-40% similarity to MAPR (membrane associated progesterone receptor) are studied in this group. The cytochrome b5 like heme/steroid binding domain are highly conserved in these proteins, and they bind progesterone and heme in animals. The UV-visible absorption spectra showed AtMAPRs are hemoproteins. (Kao, 2010, unpublished) To study the physiological role of heme-binding ability of AtMAPR3, we analyzed whether or not the expression of AtMAPR3 are subjected to the heme concentration. In this study, 10-day-old seedlings were treated with a precursor of heme, δ-aminolevulinic acid (ALA). The results showed AtMAPR3 expression was three-fold-increased by ALA treatment under 16 h light / 8 h dark, and two-fold-increased under 24 h dark; however, when adding dipyridyl (DPD), the inhibitor of Fe-chelatase, the induction was blocked. The expression of AtMAPR3 was also induced by H2O2 and tert-butyl hydroxide (tBHP) about six-fold. H2O2 could be used as a second messenger to express the defence-related genes by jasmonic acid (JA), and JA increased AtMAPR3 expression about four-fold. To further study the physiology roles of AtMAPR3, we need to analyze the phenotype of AtMAPR3-KO and other mutants. In this study, AtMAPR3-KO, AtMAPR3-OX and WT were treated with H2O2, tBHP and methyl viologen (MeV), and the survival rate of AtMAPR3-KO was lower than WT slightly. However, AtMAPR3-OX showed no differences with WT. The results revealed that the downstream products of ALA, such as Mg-protoporphyrin IX or heme, could be a signal molecule which involved in the expression of AtMAPR3. The expression of AtMAPR3 in response to ROS needs to be further investigated in physiological aspect.
author2 Chien-Chih Yang
author_facet Chien-Chih Yang
Shih-Yu Kuo
郭時鈺
author Shih-Yu Kuo
郭時鈺
spellingShingle Shih-Yu Kuo
郭時鈺
Study of the AtMAPR3 expression induced by d-amino levulinic acid and stresses in Arabidopsis
author_sort Shih-Yu Kuo
title Study of the AtMAPR3 expression induced by d-amino levulinic acid and stresses in Arabidopsis
title_short Study of the AtMAPR3 expression induced by d-amino levulinic acid and stresses in Arabidopsis
title_full Study of the AtMAPR3 expression induced by d-amino levulinic acid and stresses in Arabidopsis
title_fullStr Study of the AtMAPR3 expression induced by d-amino levulinic acid and stresses in Arabidopsis
title_full_unstemmed Study of the AtMAPR3 expression induced by d-amino levulinic acid and stresses in Arabidopsis
title_sort study of the atmapr3 expression induced by d-amino levulinic acid and stresses in arabidopsis
publishDate 2012
url http://ndltd.ncl.edu.tw/handle/2wz367
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AT guōshíyù studyoftheatmapr3expressioninducedbydaminolevulinicacidandstressesinarabidopsis
AT shihyukuo ālābójièzhōngatmapr3biǎoxiànshòudaminolevulinicacidjínìjìngyòudǎozhīyánjiū
AT guōshíyù ālābójièzhōngatmapr3biǎoxiànshòudaminolevulinicacidjínìjìngyòudǎozhīyánjiū
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