MODIFIER OF RUDIMENTARY(P1), MOD(R)(P1), A TRANS-ACTING REGULATORY MUTATION OF RUDIMENTARY

被引:8
作者
BEGLEY, D
MURPHY, AM
HIU, CH
TSUBOTA, SI
机构
[1] ST LOUIS UNIV,DEPT BIOL,ST LOUIS,MO 63103
[2] UNIV MICHIGAN,DEPT BIOL,ANN ARBOR,MI 48109
来源
MOLECULAR & GENERAL GENETICS | 1995年 / 248卷 / 01期
关键词
PYRIMIDINE BIOSYNTHESIS; REGULATION; DROSOPHILA MELANOGASTER; RUDIMENTARY GENE;
D O I
10.1007/BF02456615
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
Modifier of rudimentary(p1) (mod(r)(p1)) is a hybrid dysgenesis-induced mutation isolated as a suppresser of r(hdJ), a hypomorphic rudimentary(r) allele in Drosophila melanogaster. mod(r)(p1) has opposite effects on two of the rudimentary mutant phenotypes. It suppresses the wing truncation associated with hypomorphic r alleles, which was the phenotype used to isolate it. On the other hand, it does not suppress the sterility of r females and in fact decreases the fertility of wild-type females. This infertility is associated with a drastic decrease in r expression in mod(r)(p1) females. P element-tagging was used to clone the mutant allele, mod(r)(p1). Subsequently, 28 kb of genomic DNA encompassing the wild-type mod(r) gene in the chromosomal region 1B was cloned. mod(r) encodes a 1.3 kb transcript which is not detected in the mod(r)(p1) mutant. The sequences of mod(r) cDNA clones reveal that the gene encodes a protein of 200 amino acids in length. When compared to sequences in GenBank, the amino acid sequence did not reveal any long sequence similarities. However, the structure of the protein reveals similarities to known transcription factors. The N-terminal half of the protein is very acidic, whereas the C-terminal half is basic. The basic domain suggests a possible DNA-binding domain, while the acidic domain suggests a transcriptional activation domain. Consistent with this possibility is the fact that mod(r) acts through the 5' control region of the rudimentary gene to control its expression.
引用
收藏
页码:69 / 78
页数:10
相关论文
共 61 条
[1]   GENE-EXPRESSION DURING DROSOPHILA-MELANOGASTER OOGENESIS - ANALYSIS BY INSITU HYBRIDIZATION TO TISSUE-SECTIONS [J].
AMBROSIO, L ;
SCHEDL, P .
DEVELOPMENTAL BIOLOGY, 1984, 105 (01) :80-92
[2]   CARBAMOYL PHOSPHATE SYNTHETASE (GLUTAMINE-HYDROLYZING) - INCREASED ACTIVITY IN CANCER-CELLS [J].
AOKI, T ;
WEBER, G .
SCIENCE, 1981, 212 (4493) :463-465
[3]  
AOKI T, 1982, J BIOL CHEM, V257, P432
[4]   MUTANT ALLELES AT THE LOCUS ELAV IN DROSOPHILA-MELANOGASTER LEAD TO NERVOUS-SYSTEM DEFECTS - A DEVELOPMENTAL GENETIC-ANALYSIS [J].
CAMPOS, AR ;
GROSSMAN, D ;
WHITE, K .
JOURNAL OF NEUROGENETICS, 1985, 2 (03) :197-218
[6]   MOLECULAR-CLONING OF SUPPRESSOR OF SABLE, A DROSOPHILA-MELANOGASTER TRANSPOSON-MEDIATED SUPPRESSOR [J].
CHANG, DY ;
WISELY, B ;
HUANG, SM ;
VOELKER, RA .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (05) :1520-1528
[7]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[8]  
COULTER DE, 1990, EMBO J, V8, P3795
[9]  
DARNELL J, 1986, MOL CELL BIOL, P348
[10]   FINE STRUCTURE OF URA 2 LOCUS IN SACCHAROMYCES-CEREVISIAE .1. IN-VIVVO COMPLEMENTATION STUDIES [J].
DENISDUPHIL, M ;
LACROUTE, F .
MOLECULAR AND GENERAL GENETICS, 1971, 112 (04) :354-+