Mir1-CP, a novel defense cysteine protease accumulates in maize vascular tissues in response to herbivory

被引:62
作者
Lopez, Lorena
Camas, Alberto
Shivaji, Renuka
Ankala, Arunkanth
Williams, Paul
Luthe, Dawn
机构
[1] Penn State Univ, Dept Crop & Soil Sci, University Pk, PA 16802 USA
[2] Mississippi State Univ, Dept Biochem & Mol Biol, Mississippi State, MS 39762 USA
[3] Mississippi State Univ, Corn Host Plant Resistance Lab, USDA ARS, Mississippi State, MS 39762 USA
基金
美国国家科学基金会;
关键词
cysteine protease; induced plant defense; Spodoptera; phloem; thick-walled sieve elements; xylem; Zea; plant-herbivore interactions; mobile signal;
D O I
10.1007/s00425-007-0501-7
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
When lepidopteran larvae feed on the insect-resistant maize genotype Mp708 there is a rapid accumulation of a defensive cysteine protease, Maize insect resistance 1-cysteine protease (Mir1-CP), at the feeding site. Silver-enhanced immunolocalization visualized with both light and transmission electron microscopy was used to determine the location of Mir1-CP in the maize leaf. The results indicated that Mir1-CP is localized predominantly in the phloem of minor and intermediate veins. After 24 h of larval feeding, Mir1-CP increased in abundance in the vascular parenchyma cells and in the thick-walled sieve element (TSE); it was also found localized to the bundle sheath and mesophyll cells. In situ hybridization of mRNA encoding Mir1-CP indicated that the primary sites of Mir1-CP synthesis in the whorl are the vascular parenchyma and bundle sheath cells. In addition to the phloem, Mir1-CP was also found in the metaxylem of the leaf and root. After 24 h of foliar feeding, the amount of Mir1-CP in the root xylem increased and it appeared to move from xylem parenchyma into the root metaxylem elements. The accumulation of Mir1-CP in maize vascular elements suggests Mir1-CP may move through these tissues to defend against insect herbivores.
引用
收藏
页码:517 / 527
页数:11
相关论文
共 49 条
[11]   ALKALOID BIOGENESIS - MOLECULAR ASPECTS [J].
HASHIMOTO, T ;
YAMADA, Y .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1994, 45 :257-285
[12]   Enzymes of jasmonate biosynthesis occur in tomato sieve elements [J].
Hause, B ;
Hause, G ;
Kutter, C ;
Miersch, O ;
Wasternack, C .
PLANT AND CELL PHYSIOLOGY, 2003, 44 (06) :643-648
[13]  
Hooker J. D., 1874, NATURE, V10, P366
[14]   Phloem sap proteins: their identities and potential roles in the interaction between plants and phloem-feeding insects [J].
Kehr, J .
JOURNAL OF EXPERIMENTAL BOTANY, 2006, 57 (04) :767-774
[15]   Reversible calcium-regulated stopcocks in legume sieve tubes [J].
Knoblauch, M ;
Peters, WS ;
Ehlers, K ;
van Bel, AJE .
PLANT CELL, 2001, 13 (05) :1221-1230
[16]   Papain protects papaya trees from herbivorous insects: role of cysteine proteases in latex [J].
Konno, K ;
Hirayama, C ;
Nakamura, M ;
Tateishi, K ;
Tamura, Y ;
Hattori, M ;
Kohno, K .
PLANT JOURNAL, 2004, 37 (03) :370-378
[17]   A tomato cysteine protease required for Cf-2-dependent disease resistance and suppression of autonecrosis [J].
Krüger, J ;
Thomas, CM ;
Golstein, C ;
Dixon, MS ;
Smoker, M ;
Tang, SK ;
Mulder, L ;
Jones, JDG .
SCIENCE, 2002, 296 (5568) :744-747
[18]  
LUCAS WJ, 1994, ANNU REV PHYTOPATHOL, V32, P387, DOI 10.1146/annurev.py.32.090194.002131
[19]   cDNA cloning of a novel lectin-like xylem sap protein and its root-specific expression in cucumber [J].
Masuda, S ;
Sakuta, C ;
Satoh, S .
PLANT AND CELL PHYSIOLOGY, 1999, 40 (11) :1177-1181
[20]   An endoplasmic reticulum-derived structure that is induced under stress conditions in Arabidopsis [J].
Matsushima, R ;
Hayashi, Y ;
Kondo, M ;
Shimada, T ;
Nishimura, M ;
Hara-Nishimura, I .
PLANT PHYSIOLOGY, 2002, 130 (04) :1807-1814