Butterfly wings, a new site of porphyrin synthesis and cleavage:: Studies on the expression of the lipocalin bilin-binding protein in Pieris brassicae

被引:5
作者
Sehringer, Bernd [1 ]
Kayser, Hartmut [1 ]
机构
[1] Univ Ulm, Dept Biol 1, D-89081 Ulm, Germany
关键词
tetrapyrroles; bilin-binding protein; lipocalin; actin; glyceraldehyde-3-phosphate dehydrogenase; wing development; insects; Pieris brassicae;
D O I
10.1016/j.ibmb.2006.03.005
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 bilin-binding protein (BBP), a member of the lipocalin protein superfamily, is synthesized mainly in last instar larvae and in late pupae and newly emerged adults of Pieris brassicae, as previously reported. Here we present results from Northern blot analysis of the BBP gene transcript and from in vitro studies of holo-BBP biosynthesis with isolated wings using [C-14]5-aminolevulinic acid as a precursor to the bilin ligand, [C-14]-amino acids to label the apo-protein and inhibitors for both processes. Our combined data clearly demonstrate that BBP, which accumulates around pupa-adult transformation, is produced as holoprotein in the developing wings, while the BBP gene transcript is no longer detected in the rest of the body. Forewings and hind wings behave markedly different as the latter represent the major site of BBP? synthesis, in agreement with the unequal distribution of BBP in the wings. The presence of an active pathway of porphyrin synthesis and cleavage in insect wings, shown here for the first time, and the role of the biliprotein during wing development remains an enigma so far. As part of this work sequences of fragments of the genes for actin and glyceraldehyde-3-phosphate dehydrogenase were obtained and examined as reference house-keeping genes in the expression studies. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:482 / 491
页数:10
相关论文
共 26 条
[1]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[2]   INTERACTION OF FREE PORPHYRINS AND METALLOPORPHYRINS WITH MOUSE FERROCHELATASE - A MODEL FOR THE ACTIVE-SITE OF FERROCHELATASE [J].
DAILEY, HA ;
JONES, CS ;
KARR, SW .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 999 (01) :7-11
[3]   TOUCHDOWN PCR TO CIRCUMVENT SPURIOUS PRIMING DURING GENE AMPLIFICATION [J].
DON, RH ;
COX, PT ;
WAINWRIGHT, BJ ;
BAKER, K ;
MATTICK, JS .
NUCLEIC ACIDS RESEARCH, 1991, 19 (14) :4008-4008
[4]   PREVENTION OF NEONATAL HYPERBILIRUBINEMIA BY TIN PROTOPORPHYRIN-IX, A POTENT COMPETITIVE INHIBITOR OF HEME OXIDATION [J].
DRUMMOND, GS ;
KAPPAS, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (10) :6466-6470
[5]   The lipocalin protein family: structural and sequence overview [J].
Flower, DR ;
North, ACT ;
Sansom, CE .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2000, 1482 (1-2) :9-24
[6]  
GANFORNINA MD, 2006, IN PRESS LIPOCALINS, pCH6
[7]   THE MOLECULAR-STRUCTURE OF INSECTICYANIN FROM THE TOBACCO HORNWORM MANDUCA-SEXTA L AT 2.6 A RESOLUTION [J].
HOLDEN, HM ;
RYPNIEWSKI, WR ;
LAW, JH ;
RAYMENT, I .
EMBO JOURNAL, 1987, 6 (06) :1565-1570
[8]   MOLECULAR-STRUCTURE OF THE BILIN BINDING-PROTEIN (BBP) FROM PIERIS-BRASSICAE AFTER REFINEMENT AT 2.0-A RESOLUTION [J].
HUBER, R ;
SCHNEIDER, M ;
MAYR, I ;
MULLER, R ;
DEUTZMANN, R ;
SUTER, F ;
ZUBER, H ;
FALK, H ;
KAYSER, H .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 198 (03) :499-513
[9]   COMPARATIVE STUDIES ON THE THERMAL-STABILITY OF ANIMAL RIBOSOMAL-RNA .6. THE 28S RIBOSOMAL-RNA OF RHODNIUS-PROLIXUS IS HEAT-DISSOCIABLE ONLY AFTER ITS PURIFICATION [J].
ISHIKAWA, H ;
FILHO, WG ;
PASSOS, GAS ;
DELUCCA, FL .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1981, 68 (03) :377-381
[10]   Actin in development [J].
Jacinto, A ;
Baum, B .
MECHANISMS OF DEVELOPMENT, 2003, 120 (11) :1337-1349