THE GAPDH GENE SYSTEM OF THE RED ALGA CHONDRUS-CRISPUS - PROMOTOR STRUCTURES, INTRON-EXON ORGANIZATION, GENOMIC COMPLEXITY AND DIFFERENTIAL EXPRESSION OF GENES

被引:23
作者
LIAUD, MF
VALENTIN, C
BRANDT, U
BOUGET, FY
KLOAREG, B
CERFF, R
机构
[1] TECH UNIV CAROLO WILHELMINA BRAUNSCHWEIG,INST GENET,SPIELMANNSTR 7,D-38106 BRAUNSCHWEIG,GERMANY
[2] CTR ETUD OCEANOL BIOL MARINE,CNRS,UPR 4601,F-29682 ROSCOFF,FRANCE
关键词
CIS-ACTING ELEMENTS; INTRON CONSERVATION; INTRON SECONDARY STRUCTURE; PREMESSENGER RNA SPLICING; CPG SUPPRESSION; PROTOPLASTS; TRANSCRIPT LEVELS;
D O I
10.1007/BF00021813
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
Our previous phylogenetic analysis based on cDNA sequences of chloroplast and cytosolic glyceraldehyde-3-phosphate dehydrogenases (GAPDH; genes GapA and GapC, respectively) of the red alga Chondrus crispus suggested that rhodophytes and green plants are sister groups with respect to plastids and mitochondria and diverged at about the same time or somewhat later than animals and fungi. Here we characterize the genomic sequences of genes GapC and GapA of C. crispus with respect to promotor structures, intron/exon organization, genomic complexity, G + C content, CpG suppression and their transcript levels in gametophytes and protoplasts, respectively. To our knowledge this is the first report on nuclear protein genes of red algae. The GapC gene is G + C-rich, contains no introns and displays a number of classic sequence motifs within its promotor region, such as TATA, CAAT, GC boxes and several elements resembling the plant-specific G-box palindrome. The GapA gene has a moderate G + C content, a single CAAT box motif in its promotor region and a single intron of 115 bp near its 5' end. This intron occupies a conserved position corresponding to that of intron 1 in the transit peptide region of chloroplast GAPDH genes (GapA and GapB) of higher plants. It has consensus sequences similar to those of yeast introns and folds into a conspicuous secondary structure of -61.3 kJ. CpG profiles of genes GapC and GapA and their flanking sequences show no significant CpG depletion suggesting that these genomic sequences are not methylated. Genomic Southern blots hybridized with generic and gene specific probes indicate that both genes are encoded by single loci composed of multiple polymorphic alleles. Northern hybridizations demonstrate that both genes are expressed in gametophytes but not in protoplasts where appreciable amounts of transcripts can only be detected for GapC.
引用
收藏
页码:981 / 994
页数:14
相关论文
共 59 条
[31]   PROTOPLAST PRODUCTION IN CHONDRUS-CRISPUS GAMETOPHYTES (GIGARTINALES, RHODOPHYTA) [J].
LEGALL, Y ;
BRAUD, JP ;
KLOAREG, B .
PLANT CELL REPORTS, 1990, 8 (10) :582-585
[32]   DIFFERENTIAL INTRON LOSS AND ENDOSYMBIOTIC TRANSFER OF CHLOROPLAST GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE GENES TO THE NUCLEUS [J].
LIAUD, MF ;
ZHANG, DX ;
CERFF, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (22) :8918-8922
[33]  
LIAUD MF, 1993, ECHODYTOBIOLOGY, V5, P357
[34]  
LIAUD MF, 1993, IN PRESS J MOL EVOL
[35]  
MANIATIS T, 1982, MOL CLONING LABORATO, P270
[36]   PROKARYOTIC FEATURES OF A NUCLEUS-ENCODED ENZYME - CDNA SEQUENCES FOR CHLOROPLAST AND CYTOSOLIC GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASES FROM MUSTARD (SINAPIS-ALBA) [J].
MARTIN, W ;
CERFF, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 159 (02) :323-331
[37]   MOLECULAR EVIDENCE FOR PRE-CRETACEOUS ANGIOSPERM ORIGINS [J].
MARTIN, W ;
GIERL, A ;
SAEDLER, H .
NATURE, 1989, 339 (6219) :46-48
[38]   EVIDENCE FOR A CHIMERIC NATURE OF NUCLEAR GENOMES - EUBACTERIAL ORIGIN OF EUKARYOTIC GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE GENES [J].
MARTIN, W ;
BRINKMANN, H ;
SAVONNA, C ;
CERFF, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (18) :8692-8696
[39]  
MARTIN W, 1993, MOL BIOL EVOL, V10, P140
[40]   STRUCTURE, EVOLUTION AND ANAEROBIC REGULATION OF A NUCLEAR GENE ENCODING CYTOSOLIC GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE FROM MAIZE [J].
MARTINEZ, P ;
MARTIN, W ;
CERFF, R .
JOURNAL OF MOLECULAR BIOLOGY, 1989, 208 (04) :551-565