Homology of AFLP products in three mapping populations of barley

被引:150
作者
Waugh, R
Bonar, N
Baird, E
Thomas, B
Graner, A
Hayes, P
Powell, W
机构
[1] FED CTR BREEDING RES CULTIVATED PLANTS,INST RESISTANCE GENET,D-85461 GRUNBACH,GERMANY
[2] OREGON STATE UNIV,CORVALLIS,OR 97331
来源
MOLECULAR & GENERAL GENETICS | 1997年 / 255卷 / 03期
关键词
AFLP; barley; product homology; linkage maps;
D O I
10.1007/s004380050502
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
Segregation of 850 polymorphic AFLP (amplified fragment length polymorphism) fragments was followed in three different doubled haploid (DH) barley populations, Dicktoo x Morex (DM), Igri x Franka (IF) and Blenheim x E224/3 (BE), which had previously been used to construct linkage maps using other molecular markers. The final maps consisted of 310, 655 and 474 markers, of which 234, 194 and 376, respectively, were AFLPs. A comparison of profiles from the parental lines identified 51 similar-sized AFLPs segregating in both DM and IF populations, 20 in the DM and BE populations and 18 in the IF and BE populations. Eight segregated in all three. Analysis of the complete datasets for each of the populations using Joinmap V.2. indicated that in general terms each of the AFLPs which were polymorphic in more than one population mapped to the same genetic locus. The number of co-dominant markers segregating in a single population ranged from 6% for DM to 12.6% for IF. These results are discussed in the context of using AFLP in genetic linkage and diversity studies.
引用
收藏
页码:311 / 321
页数:11
相关论文
共 33 条
[1]  
[Anonymous], JOINMAP VERSION 2 0
[2]   IDENTIFICATION OF RAPD MARKERS LINKED TO A RHYNCHOSPORIUM-SECALIS RESISTANCE LOCUS IN BARLEY USING NEAR-ISOGENIC LINES AND BULKED SEGREGANT ANALYSIS [J].
BARUA, UM ;
CHALMERS, KJ ;
HACKETT, CA ;
THOMAS, WTB ;
POWELL, W ;
WAUGH, R .
HEREDITY, 1993, 71 :177-184
[3]   COMBINED MAPPING OF AFLP AND RFLP MARKERS IN BARLEY [J].
BECKER, J ;
VOS, P ;
KUIPER, M ;
SALAMINI, F ;
HEUN, M .
MOLECULAR & GENERAL GENETICS, 1995, 249 (01) :65-73
[4]  
Black W.C. IV, 1993, Insect Molecular Biology, V2, P1, DOI 10.1111/j.1365-2583.1993.tb00118.x
[5]   DNA AMPLIFICATION FINGERPRINTING USING VERY SHORT ARBITRARY OLIGONUCLEOTIDE PRIMERS [J].
CAETANOANOLLES, G ;
BASSAM, BJ ;
GRESSHOFF, PM .
BIO-TECHNOLOGY, 1991, 9 (06) :553-557
[6]   Detection and pattern of interspecific hybridization between Gliricidia sepium and G-maculata in Meso-America revealed by PCR-based assays [J].
Dawson, IK ;
Simons, AJ ;
Waugh, R ;
Powell, W .
MOLECULAR ECOLOGY, 1996, 5 (01) :89-98
[7]  
DEVOS KM, 1992, THEOR APPL GENET, V84, P573
[8]   Gene pool similarities of potato cyst nematode populations assessed by AFLP analysis [J].
Folkertsma, RT ;
vanderVoort, JNAMR ;
deGroot, KE ;
vanZandvoort, PM ;
Schots, A ;
Gommers, FJ ;
Helder, J ;
Bakker, J .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1996, 9 (01) :47-54
[9]   CONSTRUCTION OF AN RFLP MAP OF BARLEY [J].
GRANER, A ;
JAHOOR, A ;
SCHONDELMAIER, J ;
SIEDLER, H ;
PILLEN, K ;
FISCHBECK, G ;
WENZEL, G ;
HERRMANN, RG .
THEORETICAL AND APPLIED GENETICS, 1991, 83 (02) :250-256
[10]  
HAYES PM, 1996, P 7 INT BARL GEN S, V1, P265