MOLECULAR-CLONING AND CHROMOSOMAL LOCALIZATION OF THE MURINE HOMOLOG OF THE HUMAN HELIX-LOOP-HELIX GENE SCL

被引:87
作者
BEGLEY, CG
VISVADER, J
GREEN, AR
APLAN, PD
METCALF, D
KIRSCH, IR
GOUGH, NM
机构
[1] ROYAL MELBOURNE HOSP, DEPT DIAGNOST HAEMATOL, PARKVILLE, VIC 3050, AUSTRALIA
[2] USN, MED BRANCH, BETHESDA, MD 20814 USA
[3] NCI, PEDIAT ONCOL BRANCH, BETHESDA, MD 20814 USA
关键词
HEMATOPOIESIS; ONCOGENE; TRANSCRIPTION FACTOR; GENETIC LINKAGE; RECOMBINANT-INBRED STRAINS;
D O I
10.1073/pnas.88.3.869
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The human SCL gene is a member of the family of genes that encode the helix-loop-helix (HLH) class of DNA-binding proteins. A murine SCL cDNA was isolated from a normal macrophage cDNA library by using HLH-specific oligonucleotides as hybridization probes. The coding region is 987 base pairs and encodes a predicted protein of 34 kDa. The nucleotide sequence of the coding region shows 88% identity to the human SCL gene, and the amino acid sequence is 94% identical. The HLH motif and upstream hydrophilic region are entirely conserved in the murine and human proteins. The identity between the mouse and human sequences was less marked in the 5' and 3' untranslated regions. Two murine SCL transcripts that differ in the 3' noncoding region have been detected in fetal liver and various cell lines. Variation was also observed in the 5' untranslated region. Interestingly, immediately downstream of the protein-termination codon, both the human SCL sequence and the murine homolog share an E-box element-the suggested target site for DNA binding of HLH proteins. The murine SCL homolog was mapped to the central part of chromosomes 4.
引用
收藏
页码:869 / 873
页数:5
相关论文
共 39 条
[1]  
APLAN PD, 1990, IN PRESS MOL CELL BI
[2]   DEMONSTRATION OF DELTA-REC-PSEUDO J-ALPHA REARRANGEMENT WITH DELETION OF THE DELTA-LOCUS IN A HUMAN STEM-CELL LEUKEMIA [J].
BEGLEY, CG ;
APLAN, PD ;
DAVEY, MP ;
DEVILLARTAY, JP ;
COHEN, DI ;
WALDMANN, TA ;
KIRSCH, IR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (01) :339-342
[3]   CHROMOSOMAL TRANSLOCATION IN A HUMAN-LEUKEMIC STEM-CELL LINE DISRUPTS THE T-CELL ANTIGEN RECEPTOR DELTA-CHAIN DIVERSITY REGION AND RESULTS IN A PREVIOUSLY UNREPORTED FUSION TRANSCRIPT [J].
BEGLEY, CG ;
APLAN, PD ;
DAVEY, MP ;
NAKAHARA, K ;
TCHORZ, K ;
KURTZBERG, J ;
HERSHFIELD, MS ;
HAYNES, BF ;
COHEN, DI ;
WALDMANN, TA ;
KIRSCH, IR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (06) :2031-2035
[4]   THE GENE SCL IS EXPRESSED DURING EARLY HEMATOPOIESIS AND ENCODES A DIFFERENTIATION-RELATED DNA-BINDING MOTIF [J].
BEGLEY, CG ;
APLAN, PD ;
DENNING, SM ;
HAYNES, BF ;
WALDMANN, TA ;
KIRSCH, IR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) :10128-10132
[5]   THE PROTEIN ID - A NEGATIVE REGULATOR OF HELIX-LOOP-HELIX DNA-BINDING PROTEINS [J].
BENEZRA, R ;
DAVIS, RL ;
LOCKSHON, D ;
TURNER, DL ;
WEINTRAUB, H .
CELL, 1990, 61 (01) :49-59
[6]   2 DISTINCT MECHANISMS FOR THE SCL GENE ACTIVATION IN THE T(I-14) TRANSLOCATION OF T-CELL LEUKEMIAS [J].
BERNARD, O ;
GUGLIELMI, P ;
JONVEAUX, P ;
CHERIF, D ;
GISSELBRECHT, S ;
MAUCHAUFFE, M ;
BERGER, R ;
LARSEN, CJ ;
MATHIEUMAHUL, D .
GENES CHROMOSOMES & CANCER, 1990, 1 (03) :194-208
[7]   DAUGHTERLESS, A DROSOPHILA GENE ESSENTIAL FOR BOTH NEUROGENESIS AND SEX DETERMINATION, HAS SEQUENCE SIMILARITIES TO MYC AND THE ACHAETE-SCUTE COMPLEX [J].
CAUDY, M ;
VASSIN, H ;
BRAND, M ;
TUMA, R ;
JAN, LY ;
JAN, YN .
CELL, 1988, 55 (06) :1061-1067
[8]   A MOLECULAR GENETIC-LINKAGE MAP OF MOUSE CHROMOSOME-4 INCLUDING THE LOCALIZATION OF SEVERAL PROTO-ONCOGENES [J].
CECI, JD ;
SIRACUSA, LD ;
JENKINS, NA ;
COPELAND, NG .
GENOMICS, 1989, 5 (04) :699-709
[9]   THE TAL-GENE UNDERGOES CHROMOSOME-TRANSLOCATION IN T-CELL LEUKEMIA AND POTENTIALLY ENCODES A HELIX LOOP HELIX PROTEIN [J].
CHEN, Q ;
CHENG, JT ;
TSAI, LH ;
SCHNEIDER, N ;
BUCHANAN, G ;
CARROLL, A ;
CRIST, W ;
OZANNE, B ;
SICILIANO, MJ ;
BAER, R .
EMBO JOURNAL, 1990, 9 (02) :415-424
[10]   CELL-TYPE-SPECIFIC CONTACTS TO IMMUNOGLOBULIN ENHANCERS IN NUCLEI [J].
CHURCH, GM ;
EPHRUSSI, A ;
GILBERT, W ;
TONEGAWA, S .
NATURE, 1985, 313 (6005) :798-801