Type 1 ribosome-inactivating proteins are the most abundant proteins in iris (Iris hollandica var Professor Blaauw) bulbs: Characterization and molecular cloning

被引:33
作者
VanDamme, EJM
Barre, A
Barbieri, L
Valbonesi, P
Rouge, P
VanLeuven, F
Stirpe, F
Peumans, WJ
机构
[1] UNIV TOULOUSE 3, INST PHARMACOL & BIOL STRUCT, CNRS, UPR 9062, F-31062 TOULOUSE, FRANCE
[2] UNIV BOLOGNA, DIPARTIMENTO PATOL SPERIMENTALE, I-40126 BOLOGNA, ITALY
[3] CATHOLIC UNIV LEUVEN, CTR HUMAN GENET, B-3001 LOUVAIN, BELGIUM
关键词
D O I
10.1042/bj3240963
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The most abundant protein of Iris bulbs has been identified as a type 1 ribosome-inactivating protein (RIP). Analysis of the purified proteins and molecular cloning of the corresponding cDNAs demonstrated that this type 1 RIP is a mixture of three isoforms that exhibit a high degree of sequence identity and have similar, though not identical, ribosome-inactivating and polynucleotide :adenosine glycosidase activities. The accumulation of large quantities of type 1 RIP in a vegetative storage organ suggests that this presumed defence-related protein also plays a role in the nitrogen-storage metabolism of the bulb.
引用
收藏
页码:963 / 970
页数:8
相关论文
共 28 条
[1]  
[Anonymous], 1992, MacClade: Analysis of phylogeny and character evolution
[2]   Polynucleotide:adenosine glycosidase activity of ribosome-inactivating proteins: Effect on DNA, RNA and poly(A) [J].
Barbieri, L ;
Valbonesi, P ;
Bonora, E ;
Gorini, P ;
Bolognesi, A ;
Stirpe, F .
NUCLEIC ACIDS RESEARCH, 1997, 25 (03) :518-522
[3]   Polynucleotide:adenosine glycosidase activity of saporin-L1: Effect on DNA, RNA and poly(A) [J].
Barbieri, L ;
Valbonesi, P ;
Gorini, P ;
Pession, A ;
Stirpe, F .
BIOCHEMICAL JOURNAL, 1996, 319 :507-513
[4]   UNEXPECTED ACTIVITY OF SAPORINS [J].
BARBIERI, L ;
GORINI, P ;
VALBONESI, P ;
CASTIGLIONI, P ;
STIRPE, F .
NATURE, 1994, 372 (6507) :624-624
[5]   RIBOSOME-INACTIVATING PROTEINS FROM PLANTS [J].
BARBIERI, L ;
BATTELLI, MG ;
STIRPE, F .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1154 (3-4) :237-282
[6]   MUTAGENESIS AND KINETIC-ANALYSIS OF THE ACTIVE-SITE GLU177 OF RICIN A-CHAIN [J].
CHADDOCK, JA ;
ROBERTS, LM .
PROTEIN ENGINEERING, 1993, 6 (04) :425-431
[7]   COLORIMETRIC METHOD FOR DETERMINATION OF SUGARS AND RELATED SUBSTANCES [J].
DUBOIS, M ;
GILLES, KA ;
HAMILTON, JK ;
REBERS, PA ;
SMITH, F .
ANALYTICAL CHEMISTRY, 1956, 28 (03) :350-356
[8]   THE SITE OF ACTION OF 6 DIFFERENT RIBOSOME-INACTIVATING PROTEINS FROM PLANTS ON EUKARYOTIC RIBOSOMES - THE RNA N-GLYCOSIDASE ACTIVITY OF THE PROTEINS [J].
ENDO, Y ;
TSURUGI, K ;
LAMBERT, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 150 (03) :1032-1036
[9]   DISTRIBUTION AND PROPERTIES OF MAJOR RIBOSOME-INACTIVATING PROTEINS (28-S RIBOSOMAL-RNA N-GLYCOSIDASES) OF THE PLANT SAPONARIA-OFFICINALIS L (CARYOPHYLLACEAE) [J].
FERRERAS, JM ;
BARBIERI, L ;
GIRBES, T ;
BATTELLI, MG ;
ROJO, MA ;
ARIAS, FJ ;
ROCHER, MA ;
SORIANO, F ;
MENDEZ, E ;
STIRPE, F .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1216 (01) :31-42
[10]   HYDROPHOBIC CLUSTER-ANALYSIS - AN EFFICIENT NEW WAY TO COMPARE AND ANALYZE AMINO-ACID-SEQUENCES [J].
GABORIAUD, C ;
BISSERY, V ;
BENCHETRIT, T ;
MORNON, JP .
FEBS LETTERS, 1987, 224 (01) :149-155