scholarly journals Genetic linkage in soybean : Linkage Group 8

1992 ◽  
Author(s):  
Kimberly Haack
Genomics ◽  
2006 ◽  
Vol 87 (1) ◽  
pp. 1-29 ◽  
Author(s):  
June E. Swinburne ◽  
Mike Boursnell ◽  
Gemma Hill ◽  
Louise Pettitt ◽  
Twink Allen ◽  
...  

Genome ◽  
2014 ◽  
Vol 57 (3) ◽  
pp. 155-160 ◽  
Author(s):  
Yang Yang ◽  
Benjamin D. Speth ◽  
Napatsakorn Boonyoo ◽  
Eric Baumert ◽  
Taylor R. Atkinson ◽  
...  

In soybean, an environmentally stable male sterility system is vital for making hybrid seed production commercially viable. Eleven male-sterile, female-fertile mutants (ms1, ms2, ms3, ms4, ms5, ms6, ms7, ms8, ms9, msMOS, and msp) have been identified in soybean. Of these, eight (ms2, ms3, ms5, ms7, ms8, ms9, msMOS, and msp) have been mapped to soybean chromosomes. The objectives of this study were to (i) locate the ms1, ms4, and ms6 genes to soybean chromosomes; (ii) generate genetic linkage maps of the regions containing these genes; and (iii) develop a comprehensive map of all known male-sterile, female-fertile genes in soybean. The bulked segregant analysis technique was used to locate genes to soybean chromosomes. Microsatellite markers from the corresponding chromosomes were used on F2 populations to generate genetic linkage maps. The ms1 and ms6 genes were located on chromosome 13 (molecular linkage group F) and ms4 was present on chromosome 2 (molecular linkage group D1b). Molecular analyses revealed markers Satt516, BARCSOYSSR_02_1539, and AW186493 were located closest to ms1, ms4, and ms6, respectively. The ms1 and ms6 genes, although present on the same chromosome, were independently assorting with a genetic distance of 73.7 cM. Using information from this study and compiled information from previously published male sterility genes in soybean, a comprehensive genetic linkage map was generated. Eleven male sterility genes were present on seven soybean chromosomes. Four genes were present in two regions on chromosome 2 (molecular linkage group D1b) and two genes were present on chromosome 13 (molecular linkage group F).


Genome ◽  
2008 ◽  
Vol 51 (8) ◽  
pp. 628-637 ◽  
Author(s):  
S. K. Gupta ◽  
J. Souframanien ◽  
T. Gopalakrishna

A genetic linkage map of black gram, Vigna mungo (L.) Hepper, was constructed with 428 molecular markers using an F9 recombinant inbred population of 104 individuals. The population was derived from an inter-subspecific cross between a black gram cultivar, TU94-2, and a wild genotype, V. mungo var. silvestris. The linkage analysis at a LOD score of 5.0 distributed all 428 markers (254 AFLP, 47 SSR, 86 RAPD, and 41 ISSR) into 11 linkage groups. The map spanned a total distance of 865.1 cM with an average marker density of 2 cM. The largest linkage group spanned 115 cM and the smallest linkage group was of 44.9 cM. The number of markers per linkage group ranged from 11 to 86 and the average distance between markers varied from 1.1 to 5.6 cM. Comparison of the map with other published azuki bean and black gram maps showed high colinearity of markers, with some inversions. The current map is the most saturated map for black gram to date and will provide a useful tool for identification of QTLs and for marker-assisted selection of agronomically important characters in black gram.


Genetics ◽  
1995 ◽  
Vol 139 (4) ◽  
pp. 1727-1735 ◽  
Author(s):  
S L Johnson ◽  
D Africa ◽  
S Horne ◽  
J H Postlethwait

Abstract Analysis of meiotic tetrads is routinely used to determine genetic linkage in various fungi. Here we apply tetrad analysis to the study of genetic linkage in a vertebrate. The half-tetrad genotypes of gynogenetic diploid zebrafish produced by early-pressure (EP) treatment were used to investigate the linkage relationships of two recessive pigment pattern mutations, leopard (leo) and rose (ros). The results showed that ros is tightly linked to its centromere and leo maps 31 cM from its centromere. Analysis of half-tetrads segregating for ros and leo in repulsion revealed no homozygous ros individuals among 32 homozygous leo half-tetrads--i.e., a parental ditype (PD) to nonparental ditype (NPD) ratio of 32:0. This result shows that ros is linked to leo, a mutation previously mapped to Linkage Group I. Investigation of PCR-based DNA polymorphisms on Linkage Group I confirmed the location of ros near the centromere of this linkage group. We propose an efficient, generally useful method to assign new mutations to a linkage group in zebrafish by determining which of 25 polymerase chain reaction (PCR)-based centromere markers shows a significant excess of PD to NPD in half-tetrad fish.


Crop Science ◽  
1989 ◽  
Vol 29 (3) ◽  
pp. 698-700 ◽  
Author(s):  
P. R. Thorson ◽  
B. R. Hedges ◽  
R. G. Palmer

Genome ◽  
1987 ◽  
Vol 29 (4) ◽  
pp. 582-583 ◽  
Author(s):  
Y. T. Kiang ◽  
Y. C. Chiang

Four crosses were made among seven soybean cultivars for determining possible linkage between Adh1 and W1 loci. An examination of F2 seed indicated that these loci are linked with a recombination value of 20.6 ± 1.2%. These loci are located in linkage group 8. Key words: soybean linkage, isozymes, alcohol dehydrogenase (Adh1), color locus (W1), Glycine max.


1990 ◽  
Vol 54 (1-2) ◽  
pp. 95-96 ◽  
Author(s):  
J. Nguyen ◽  
P. Charmley ◽  
W.W. Grody ◽  
S.D. Cederbaum ◽  
M.-C. King ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document