Fast Neutron Mutagenesis of Soybean (Glycine soja L.) Produces a Supernodulating Mutant Containing a Large Deletion in Linkage Group H

2002 ◽  
Vol 1 (3) ◽  
pp. 147-155 ◽  
Author(s):  
Artem E. Men ◽  
Titeki S. Laniya ◽  
Iain R. Searle ◽  
Inaki Iturbe-Ormaetxe ◽  
Irma Gresshoff ◽  
...  
Genetics ◽  
1998 ◽  
Vol 149 (3) ◽  
pp. 1575-1585
Author(s):  
Edward P Bruggemann ◽  
Bernard Doan ◽  
Korie Handwerger ◽  
Gisela Storz

Abstract The Arabidopsis HY4 gene encodes the nonessential blue light photoreceptor CRY1. Loss-of-function hy4 mutants have an elongated hypocotyl phenotype after germination under blue light. We previously analyzed 20 independent hy4 alleles produced by fast neutron mutagenesis. These alleles were grouped into two classes based on their genetic behavior and corresponding deletion size: (1) null hy4 alleles that were semidominant over wild type and contained small or moderate-sized deletions at HY4 and (2) null hy4 alleles that were recessive lethal and contained large HY4 deletions. Here we describe one additional fast neutron hy4 mutant, B144, that did not fall into either of these two classes. Mutant B144 was isolated as a heterozygote with an intermediate hy4 phenotype. One allele from this mutant, hy4-B144Δ, contains a large deletion at HY4 and is recessive lethal. The other allele from this mutant, HY4-B144*, appears to be intact and functional but is unstable and spontaneously converts to a nonfunctional hy4 allele. In addition, HY4-B144* is lethal in homozygotes and suppresses local recombination. We discuss genetic and epigenetic mechanisms that may account for the unusual behavior of the HY4-B144* allele.


Genome ◽  
1987 ◽  
Vol 29 (5) ◽  
pp. 786-792 ◽  
Author(s):  
Y. C. Chiang ◽  
Y. T. Kiang

The inheritance of 6-phosphogluconate dehydrogenase (6-PGD) in dry seeds of cultivated and wild soybean was studied electrophoretically. There are four 6-PGD anodal bands that are controlled by three loci. Bands 1 and 3 are homodimers, whereas band 2 is the interlocus heterodimer of bands 1 and 3, which are products of the Pgd1 and Pgd2 loci, respectively. Both Pgd1 and Pgd2 loci have three codominant alleles (Pgd1-a, Pgd1-b, Pgd1-c and Pgd2-a, Pgd2-b, Pgd2-c) and each of the alleles specifies an isozyme band. The two variants of the fourth band are the result of two codominant alleles (Pgd3-a and Pgd3-b) of the Pgd3 locus. The Pgd3-a allele is found only in PI486.220, a Glycine soja accession from Japan. The Pgd2 is linked to Ap, Ti, and Lap1 in the order of Ap–Ti–Lap1–Pgd2 and belongs to linkage group 9. Key words: soybean isozymes linkage, genetics of Pgd loci.


Author(s):  
Robert C. Rau ◽  
Robert L. Ladd

Recent studies have shown the presence of voids in several face-centered cubic metals after neutron irradiation at elevated temperatures. These voids were found when the irradiation temperature was above 0.3 Tm where Tm is the absolute melting point, and were ascribed to the agglomeration of lattice vacancies resulting from fast neutron generated displacement cascades. The present paper reports the existence of similar voids in the body-centered cubic metals tungsten and molybdenum.


Author(s):  
T. Y. Tan ◽  
W. K. Tice

In studying ion implanted semiconductors and fast neutron irradiated metals, the need for characterizing small dislocation loops having diameters of a few hundred angstrom units usually arises. The weak beam imaging method is a powerful technique for analyzing these loops. Because of the large reduction in stacking fault (SF) fringe spacing at large sg, this method allows for a rapid determination of whether the loop is faulted, and, hence, whether it is a perfect or a Frank partial loop. This method was first used by Bicknell to image small faulted loops in boron implanted silicon. He explained the fringe spacing by kinematical theory, i.e., ≃l/(Sg) in the fault fringe in depth oscillation. The fault image contrast formation mechanism is, however, really more complicated.


2001 ◽  
Vol 32 (5) ◽  
pp. 321-321 ◽  
Author(s):  
S. M. Schmutz ◽  
J. S. Moker ◽  
V. Yuzbasiyan-Gurkan ◽  
D. Zemke ◽  
J. Sampson ◽  
...  
Keyword(s):  

2003 ◽  
Vol 8 (5-6) ◽  
pp. 106-110 ◽  
Author(s):  
I.I. Zalyubovsky ◽  
◽  
V.M. Kartashev ◽  
V.E. Kovtun ◽  
O.K. Minko ◽  
...  

1972 ◽  
Vol 12 ◽  
pp. 11-32 ◽  
Author(s):  
W. Duncan

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 547b-547
Author(s):  
Soon O. Park ◽  
Dermot P. Coyne ◽  
Geunhwa Jung ◽  
E. Arnaud-Santana ◽  
H. Ariyarathne

Seed size is an important trait in common bean. The objective was to identify RAPD markers associated with QTL for seed weight, seed length, and seed height in a molecular marker-based linkage map in a recombinant inbred (RI) population from the common bean cross of the larger seeded (100 seed/39 to 47 g) PC-50 (ovate seed shape) × smaller seeded (100 seed/26 to 35 g) XAN-159 (flat rhomboidal seed shape). The parents and RI lines were grown in two separate greenhouse and two field (Wisconsin, Dominican Republic) experiments using a RCBD. Continuous distributions for seed weight, seed length, and seed height were observed for RI lines indicating quantitative inheritance. One to three QTLs affecting seed weight explained 17% to 41% of the phenotypic variation. Two to three QTLs for seed length explained 23% to 45% of the phenotypic variation. One to four QTL associated with seed height explained 17% to 39% of the phenotypic variation. A RAPD marker M5.850 in linkage group 3 was consistently associated with seed weight, seed length, and seed height in all experiments and explained 7% to 13% of the phenotypic variation for these traits. A seedcoat pattern morphological marker (C) in linkage group 1 was associated with seed weight and seed height in two greenhouse experiments.


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