DEFOG: A practical scheme for deciphering families of genes

被引:16
作者
Fuchs, T
Malecova, B
Linhart, C
Sharan, R
Khen, M
Herwig, R
Shmulevich, D
Elkon, R
Steinfath, M
O'Brien, JK
Radelof, U
Lehrach, H
Lancet, D
Shamir, R [1 ]
机构
[1] Tel Aviv Univ, Sackler Fac Exact Sci, Sch Comp Sci, IL-69978 Tel Aviv, Israel
[2] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[3] Weizmann Inst Sci, Crown Human Genome Ctr, IL-76100 Rehovot, Israel
[4] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[5] Tel Aviv Univ, Sackler Fac Exact Sci, David & Inez Lab Genet Res, Dept Human Genet & Mol Med, IL-69978 Tel Aviv, Israel
[6] Royal Coll Surgeons Ireland, Dept Clin Pharmacol, Dublin 2, Ireland
关键词
gene family; olfactory receptors; degenerate primers; clustering; oligonucleotide fingerprinting;
D O I
10.1006/geno.2002.6830
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
We developed a novel efficient scheme, DEFOG (for "deciphering families of genes"), for determining sequences of numerous genes from a family of interest. The scheme provides a powerful means to obtain a gene family composition in species for which high-throughput genomic sequencing data are not available. DEFOG uses two key procedures. The first is a novel algorithm for designing highly degenerate primers based on a set of known genes from the family of interest. These primers are used in PCR reactions to amplify the members of the gene family. The second combines oligofingerprinting of the cloned PCR products with clustering of the clones based on their fingerprints. By selecting members from each cluster, a low-redundancy clone subset is chosen for sequencing. We applied the scheme to the human olfactory receptor (OR) genes. OR genes constitute the largest gene superfamily in the human genome, as well as in the genomes of other vertebrate species. DEFOG almost tripled the size of the initial repertoire of human ORs in a single experiment, and only 7% of the PCR clones had to be sequenced. Extremely high degeneracies, reaching over a billion combinations of distinct PCR primer pairs, proved to be very effective and yielded only 0.4% nonspecific products.
引用
收藏
页码:295 / 302
页数:8
相关论文
共 39 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   Genomic structure and transcription of a murine odorant receptor gene: Differential initiation of transcription in the olfactory and testicular cells [J].
Asai, H ;
Kasai, H ;
Matsuda, Y ;
Yamazaki, N ;
Nagawa, F ;
Sakano, H ;
Tsuboi, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 221 (02) :240-247
[3]   A NOVEL MULTIGENE FAMILY MAY ENCODE ODORANT RECEPTORS - A MOLECULAR-BASIS FOR ODOR RECOGNITION [J].
BUCK, L ;
AXEL, R .
CELL, 1991, 65 (01) :175-187
[4]   The olfactory multigene family [J].
Buck, Linda B. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1992, 2 (03) :467-473
[5]  
Clark MD, 1999, METHOD ENZYMOL, V303, P205
[6]  
DAYHOFF MO, 1976, FED PROC, V35, P2132
[7]  
Everitt B., 1993, CLUSTER ANAL
[8]   The human olfactory subgenome: from sequence to structure and evolution [J].
Fuchs, T ;
Glusman, G ;
Horn-Saban, S ;
Lancet, D ;
Pilpel, Y .
HUMAN GENETICS, 2001, 108 (01) :1-13
[9]   The olfactory receptor gene superfamily: data mining, classification, and nomenclature [J].
Glusman, G ;
Bahar, A ;
Sharon, D ;
Pilpel, Y ;
White, J ;
Lancet, D .
MAMMALIAN GENOME, 2000, 11 (11) :1016-1023
[10]   The complete human olfactory subgenome [J].
Glusman, G ;
Yanai, I ;
Rubin, I ;
Lancet, D .
GENOME RESEARCH, 2001, 11 (05) :685-702