Lectin protein and Kunitz trypsin inhibitor (KTI) protein of mature 　soybean seed are a main antinutritional factor in soybean seed. The Le gene controls a lectin protein and Ti gene controls the KTI protein in soybean. Ti locus has been located on linkage group 9 in the classical linkage map of soybean. Position of Le locus on linkage map was not identified. Genetic relationship between Ti locus and Le locus could be useful in soybean breeding program for the genetic elimination of these factors. The objective of this study was to determine the independent inheritance or linkage between Ti locus and Le locus in soybean seed. Two F2 populations were developed from three parents (Gaechuck#1, T102, and PI548415). The F1 seeds from Gaechuck#1 (titiLeLe) x T102 (TiTilele) and Gaechuck#1 (titiLeLe) x PI548415 (TiTilele) were obtained. The lectin and KTI protein were analysed from F2 seeds harvested from the F1 plants to find independent assortment or linkage between Ti locus and Le locus. The segregation ratios of 3 : 1 for Le locus (129 Le_ : 44 lele) and Ti locus (132 Ti_ : 41 titi) and were observed. The segregation ratios of 9 : 3 : 3 : 1 (95 Le_Li_ : 34 Le_titi: 37 leleTi_ : 7 leletiti) between Le gene and Ti gene in F2 seeds were observed. This data showed that Ti gene was inherited independently with the Le gene in soybean. These results will be helpful in breeding program for selecting the line with lacking both KTI and lectin protein in soybean.

dlm mutants controlling disease lesion mimic leaf trait may be useful in basic research of disease hypersensitive response and programmed cell death in soybean. The study on genetic relationship between dlm trait and other morphological C trait, position of dlm allele on classical linkage group, and a molecular marker linked to dlm allele was little reported. Two populations [T173 (ffDlmDlm) x T363 (FFdlmdlm), T363 (dlmdlmY9Y9) x T135 (DlmDlmy9y9)] were made to find independent assortment or linkage between dlm locus and f locus or between dlm locus and y9 locus. The segregation ratios of 3 : 1 were observed in the F2 population and the Chi-square values suggested that the disease lesion mimic leaf, fasciation stem, and chlorophyll-deficient leaf traits were controlled by a single recessive gene. Segregation ratios of 78 Dlm_F_: 19 Dlm_ff: 17 dlmdlmF_ : 3 dlmdlmff based on F2 phenotype showed that dlm allele was inherited independently with the f allele controlling fasciation stem trait in soybean. Also, segregation ratios of from 149 Dlm_Y9_: 41 Dlm_y9y9: 38 dlmdlmY9_ : 5 dlmdlmy9y9 based on F2 phenotype confirmed that dlm allele was inherited independently with the y9 allele controlling chlorophyll- deficient leaf trait in soybean. From these results, dlm allele would not be located on linkage group 11 (molecular linkage group: D1b+W) and linkage group 14 (molecular linkage group: E) in soybean. This results will helpful to attempt to position the Dlm locus on the soybean molecular linkage map.

dlm allele controlling disease lesion mimic trait is useful in basic research aimed at better understanding disease hypersensitive response and programmed cell death in soybean. Inheritance between dlm trait and any morphological trait, position of dlm allele on classical linkage group, molecular marker linked to dlm allele were not reported. Two populations [T255 (lf2lf2DlmDlm) x T363 (Lf2Lf2dlmdlm), T363 (dlmdlmp1p1) x T43 (DlmDlmP1P1)] were made to find independent assortment or linkage between dlm locus and lf2 or between dlm locus and P1 locus. The segregation ratios of 3 : 1 were observed in the F2 population and the Chi-square values strongly suggested that the disease lesion mimic and seven-leaflet trait was controlled by a single recessive gene. Glabrousness trait was controlled by a single dominant gene. Segregation ratios of 48 Lf2_Dlm_: 30 Lf2_dlmdlm: 21 lf2f2Dlm_ : 8 lf2lf2dlmdlm based on F2 phenotype showed that dlm allele was inherited independently with the lf2 allele controlling seven-leaflet trait in soybean. However, more F2 plants will be needed to confirm this result. Also, segregation ratios of 137 P1_Dlm_: 46 P1_dlmdlm: 49 p1p1Dlm_ : 16 p1p1dlmdlm from F2 phenotype confirmed strongly that dlm allele was inherited independently with the P1 allele controlling glabrous trait in soybean. This results indicate that dlm allele will not located in soybean classical linkage group 2 (molecular linkage group K) and soybean classical linkage group 16. This observation will helpful to attempt to position the Dlm locus on the soybean molecular linkage map.

Isoflavone is synthesized in several different organs such as root, leaf and developing and germinating seed. Isoflavone content reflects overall history of physiological event given to a plant during certain period of time. Amount of isoflavone in a orga

Leaflet number of soybean controlled by Lf2 locus is the important trait in photosynthesis and plant type. The objective of this research was to identity molecular markers linked to the lf2 locus. A total of 115F2 plants were derived from a cross between normal three-leaflet type Sinpaldalkong (Lf2Lf2) and seven-leaflet mutant type T255 (lf2lf2). All leaflet counts of parents and F2 individual plants were made in the field on fully expanded leaves on the main stem when terminal growth of the main stem had ceased. One-thousand 10-mer oligonucleotide RAPD primers and 664 SSR primers were used. The segregation ratios of 3 : 1 were observed in the F2 population and the Chi-square values strongly suggested that the seven-leaflet was controlled by a single recessive gene. A genetic map was constructed from the 15 segregating markers (9 RAPDs, 5 SSRs, 1 lf2 locus). OPAD03 and OPAI13 RAPD markers were linked to the lf2 locus that controlled seven-leaflet type at a distance of 20.5 and 23.5 cM, respectively. Molecular markers identified in this study linked with lf2 locus will be helpful to locate lf2 locus on the public soybean molecular linkage map and would be useful for tagging the lf2 locus that controls seven-leaflet trait.

Leaf chlorophyll-deficient mutants controlled by y9 locus have been observed frequently and are useful in genetic stud-y9 locus. A mapping population con-sisting of 94 F2 progeny was derived from a cross between normal green leaf Clark (Y9 ) and chlorophy

Soybean seeds contain high amounts of isoflavones that display biological effects and isoflavone content of soybean seed can vary by year, environment, and genotype. Objective of this study was to identify quantitative trait loci that underlie isoflavone content in soybean seeds. The study involved 85 F2 populations derived from Korean soybean cultivar 'Kwangkyo' and wild type soybean 'IT182305' for QTL analysis associated with isoflavone content. Isoflavone content of seeds was determined by HPLC. The genetic map of 33 linkage groups with 207 markers was constructed. The linkage map spanned 2,607.5 cM across all 33 linkage groups. The average linkage distance between pair of markers among all linkage groups was 12.6 cM in Kosambi map units. Isoflavone content in F2 generations varied in a fashion that suggested a continuous, polygenic inheritance. Eleven markers (4 RAPD, 3 SSR, 4 AFLP) were significantly associated with isoflavone content. Only two markers, Satt419 and CTCGAG3 had F-tests that were significant at P<0.01 in F2 generation for isoflavone content. Interval mapping using the F2 data revealed only two putative QTLs for isoflavone content. The peak QTL region on linkage group 3, which was near OPAG03c, explained 14~% variation for isoflavone content. The peak QTL region on linkage group 5, which was located near OPN14 accounted for 35.3~% variation for isoflavone content. Using both Map-Maker-QTL (LOD~geq2.0) and single-factor analysis (P~leq0.05) , one marker, CTCGAG3 in linkage group 3 was associated with QTLs for isoflavone content. This information would then be used in identification of QTLs for isoflavone content with precision

Soybean is a major source of protein meal in the world. Kunitz trypsin inhibitor (KTI) protein is responsible for the inferior nutritional quality of unheated or incompletely heated soybean meal. The objective of this research was to identify RAPD markers linked to KTI protein allele using bulked segregant analysis. Cultivar Jinpumkong2 (TiTi) was crossed with C242 (titi, absence of KTI protein) and F. seeds were planted. The F1 . plants were grown in the greenhouse to produce F2 seeds. Each F2 seed from F1 . plants was analysed electrophoretically to determine the presence of the KTI protein band. The present and absent bulks contained twenty individuals each, which were selected on the basis of the KTI protein electrophoresis, respectively. Total 94 F2 individuals were constructed and 1,000 Operon random primers were used to identify RAPD primers linked to the Ti locus. The presence of KTI protein is dominant to the lack of a KTI protein and Kunitz trypsin inhibit protein band is controlled by a single locus. Four RAPD primers (OPAC12, OPAR15, OPO12, and OPC08) were linked to the Ti locus. RAPD primer OPO12 was linked to Ti locus, controlling kunitz trypsin inhibitor protein at a distance of 16.0 cM. This results may assist in study of developing fine map including Ti locus in soybean.

Genetic linkage maps serve the plant geneticist in a number of ways, from marker assisted selection in plant improvement to map-based cloning in molecular genetic research. Genetic map based upon DNA polymorphism is a powerful tool for the study of qualitative and quantitative traits in crops. The objective of this study was to develop genetic linkage map of soybean using the population derived from the cross of Korean soybean cultivar 'Kwangkyo, and wild accession 'IT182305'. Total 1,000 Operon random primers for RAPD marker, 49 combinations of primer for AFLP marker, and 100 Satt primers for SSR marker were used to screen parental polymorphism. Total 341 markers (242 RAPD, 83 AFLP, and 16 SSR markers) was segregated in 85 ~textrmF2 population. Forty two markers that shown significantly distorted segregation ratio (1:2:1 for codominant or 3:1 for domimant marker) were not used in mapping procedure. A linkage map was constructed by applying the computer program MAPMAKER/EXP 3.0 to the 299 marker data with LOD 4.0 and maximum distance 50 cM. 176 markers were found to be genetically linked and formed 25 linkage groups. Linkage map spanned 2,292.7 cM across all 25 linkage groups. The average linkage distance between pair of markers among all linkage groups was 13.0 cM. The number of markers per linkage group ranged from 2 to 55. The longest linkage group 3 spanned 967.4 cM with 55 makers. This map requires further saturation with more markers and agronomically important traits will be joined over it.