GENOMIC ORGANIZATION OF THE NEUROFIBROMATOSIS-1 GENE (NF1)

被引:191
作者
LI, Y
OCONNELL, P
BREIDENBACH, HH
CAWTHON, R
STEVENS, J
XU, GF
NEIL, S
ROBERTSON, M
WHITE, R
VISKOCHIL, D
机构
[1] UNIV UTAH, DEPT PEDIAT, DIV MED GENET, SALT LAKE CITY, UT 84112 USA
[2] UNIV UTAH, ECCLES INST HUMAN GENET, DEPT HUMAN GENET, SALT LAKE CITY, UT 84112 USA
关键词
D O I
10.1016/0888-7543(95)80104-T
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Neurofibromatosis 1 maps to chromosome band 17q11.2, and the NF1 locus has been partially characterized. Even though the full-length NF1 cDNA has been sequenced, the complete genomic structure of the NF1 gene has not been elucidated, The 5' end of NF1 is embedded in a CpG island containing a NotI restriction site, and the remainder of the gene lies in the adjacent 350-kb NotI fragment. In our efforts to develop a comprehensive screen for NF1 mutations, we have isolated genomic DNA clones that together harbor the entire NF1 cDNA sequence. We have identified all intron-exon boundaries of the coding region and established that it is composed of 59 exons. Furthermore, we have defined the 3'-untranslated region (3'-UTR) of the NF1 gene; it spans approximately 3.5 kb of genomic DNA sequence and is continuous with the stop codon. Oligonucleotide primer pairs synthesized from exon-flanking DNA sequences were used in the polymerase chain reaction with cloned, chromosome 17-specific genomic DNA as template to amplify NF1 exons 1 through 27b and the exon containing the 3'-UTR separately. This information should be useful for implementing a comprehensive NF1 mutation screen using genomic DNA as template. (C) 1995 Academic Press, Inc.
引用
收藏
页码:9 / 18
页数:10
相关论文
共 41 条
[21]  
Martin-Gallardo A, 1992, DNA Seq, V3, P237, DOI 10.3109/10425179209034023
[22]  
NISHI T, 1991, ONCOGENE, V6, P1555
[23]  
OCHMAN H, 1988, GENETICS, V120, P621
[24]   THE HUMAN HOMOLOG OF MURINE EVI-2 LIES BETWEEN 2 VONRECKLINGHAUSEN NEUROFIBROMATOSIS TRANSLOCATIONS [J].
OCONNELL, P ;
VISKOCHIL, D ;
BUCHBERG, AM ;
FOUNTAIN, J ;
CAWTHON, RM ;
CULVER, M ;
STEVENS, J ;
RICH, DC ;
LEDBETTER, DH ;
WALLACE, M ;
CAREY, JC ;
JENKINS, NA ;
COPELAND, NG ;
COLLINS, FS ;
WHITE, R .
GENOMICS, 1990, 7 (04) :547-554
[25]   2 NF1 TRANSLOCATIONS MAP WITHIN A 600-KILOBASE SEGMENT OF 17Q11.2 [J].
OCONNELL, P ;
LEACH, R ;
CAWTHON, RM ;
CULVER, M ;
STEVENS, J ;
VISKOCHIL, D ;
FOURNIER, REK ;
RICH, DC ;
LEDBETTER, DH ;
WHITE, R .
SCIENCE, 1989, 244 (4908) :1087-1088
[26]  
PIERCE JC, 1992, METHOD ENZYMOL, V216, P549
[27]   GENETIC COMPLEMENTATION REVEALS A NOVEL REGULATORY ROLE FOR 3' UNTRANSLATED REGIONS IN GROWTH AND DIFFERENTIATION [J].
RASTINEJAD, F ;
BLAU, HM .
CELL, 1993, 72 (06) :903-917
[28]  
ROUX KH, 1990, BIOTECHNIQUES, V8, P48
[29]   PRIMER-DIRECTED ENZYMATIC AMPLIFICATION OF DNA WITH A THERMOSTABLE DNA-POLYMERASE [J].
SAIKI, RK ;
GELFAND, DH ;
STOFFEL, S ;
SCHARF, SJ ;
HIGUCHI, R ;
HORN, GT ;
MULLIS, KB ;
ERLICH, HA .
SCIENCE, 1988, 239 (4839) :487-491
[30]  
Sambrook J., 1989, MOL CLONING LAB MANU