Mapping barley genes to chromosome arms by transcript profiling of wheat–barley ditelosomic chromosome addition lines

Genome ◽  
2007 ◽  
Vol 50 (10) ◽  
pp. 898-906 ◽  
Author(s):  
Hatice Bilgic ◽  
Seungho Cho ◽  
David F. Garvin ◽  
Gary J. Muehlbauer

Wheat–barley disomic and ditelosomic chromosome addition lines have been used as genetic tools for a range of applications since their development in the 1980s. In the present study, we used the Affymetrix Barley1 GeneChip for comparative transcript analysis of the barley cultivar Betzes, the wheat cultivar Chinese Spring, and Chinese Spring – Betzes ditelosomic chromosome addition lines to physically map barley genes to their respective chromosome arm locations. We mapped 1257 barley genes to chromosome arms 1HS, 2HS, 2HL, 3HS, 3HL, 4HS, 4HL, 5HS, 5HL, 7HS, and 7HL based on their transcript levels in the ditelosomic addition lines. The number of genes assigned to individual chromosome arms ranged from 24 to 197. We validated the physical locations of the genes through comparison with our previous chromosome-based physical mapping, comparative in silico mapping with rice and wheat, and single feature polymorphism (SFP) analysis. We found our physical mapping of barley genes to chromosome arms to be consistent with our previous physical mapping to whole chromosomes. In silico comparative mapping of barley genes assigned to chromosome arms revealed that the average genomic synteny to wheat and rice chromosome arms was 63.2% and 65.5%, respectively. In the 1257 mapped genes, we identified SFPs in 924 genes between the appropriate ditelosomic line and Chinese Spring that supported physical map placements. We also identified a single small rearrangement event between rice chromosome 9 and barley chromosome 4H that accounts for the loss of synteny for several genes.

Genetics ◽  
2000 ◽  
Vol 156 (1) ◽  
pp. 327-339 ◽  
Author(s):  
O Riera-Lizarazu ◽  
M I Vales ◽  
E V Ananiev ◽  
H W Rines ◽  
R L Phillips

Abstract In maize (Zea mays L., 2n = 2x = 20), map-based cloning and genome organization studies are often complicated because of the complexity of the genome. Maize chromosome addition lines of hexaploid cultivated oat (Avena sativa L., 2n = 6x = 42), where maize chromosomes can be individually manipulated, represent unique materials for maize genome analysis. Maize chromosome addition lines are particularly suitable for the dissection of a single maize chromosome using radiation because cultivated oat is an allohexaploid in which multiple copies of the oat basic genome provide buffering to chromosomal aberrations and other mutations. Irradiation (gamma rays at 30, 40, and 50 krad) of a monosomic maize chromosome 9 addition line produced maize chromosome 9 radiation hybrids (M9RHs)—oat lines possessing different fragments of maize chromosome 9 including intergenomic translocations and modified maize addition chromosomes with internal and terminal deletions. M9RHs with 1 to 10 radiation-induced breaks per chromosome were identified. We estimated that a panel of 100 informative M9RHs (with an average of 3 breaks per chromosome) would allow mapping at the 0.5- to 1.0-Mb level of resolution. Because mapping with maize chromosome addition lines and radiation hybrid derivatives involves assays for the presence or absence of a given marker, monomorphic markers can be quickly and efficiently mapped to a chromosome region. Radiation hybrid derivatives also represent sources of region-specific DNA for cloning of genes or DNA markers.


1980 ◽  
Vol 36 (3) ◽  
pp. 311-325 ◽  
Author(s):  
Gary E. Hart ◽  
A. K. M. R. Islam ◽  
K. W. Shepherd

SUMMARYThe alcohol dehydrogenase (ADH), glutamic oxaloacetic transaminase (GOT), aminopeptidase (AMP), endopeptidase (EP), and esterase (EST) zymogram phenotypes of Chinese Spring wheat, Betzes barley, Chinese Spring-Betzes heptaploids, and a number of presumptive Betzes chromosome additions to Chinese Spring were determined. It was found that four disomic chromosome addition lines could be distinguished from one another and from the other three possible lines on the basis of the zymogram phenotypes of these isozymes.The structural gene Adh-H1 was located in Betzes chromosome 4, the genes Got-H2 and Amp-H1 in chromosome 6, and the gene Ep-H1 in chromosome 1. These gene locations provide evidence of homoeology between Betzes chromosomes 4, 6, and 1 and the Chinese Spring chromosomes of homoeologous groups 4, 6, and 7, respectively.


Genome ◽  
1988 ◽  
Vol 30 (4) ◽  
pp. 519-524 ◽  
Author(s):  
N. A. Tuleen ◽  
G. E. Hart

Isozyme markers were used to develop Triticum aestivum cv. Chinese Spring–Elytrigia elongata (= Agropyron elongatum, 2n = 14, genome E) disomic 3E and 5E addition lines. Subsequently, all possible lines containing 3E and 5E substituted for wheat homoeologues and several 3E and 5E ditelosomic addition and substitution lines were developed. Plants containing chromosome 3E substituted for wheat chromosomes of homoeologous group 3 are similar to 'Chinese Spring' in vigor and fertility while plants containing 3EL substituted for chromosomes of group 3 are less fertile than 'Chinese Spring'. This indicates that both arms of 3E are involved in sporophytic compensation. Plants containing chromosome 5E substituted for wheat chromosomes of homoeologous group 5 are as vigorous but less fertile than 'Chinese Spring'. 5EL (5A) and 5EL (5B) plants are lower in fertility than 5E (5A) and 5E (5B) plants, indicating that both arms of 5E are involved in sporophytic compensation. 5E (5D) and 5EL (5D) plants are similar in fertility. Male gametophytes in which 3E or 5E replaces a wheat homoeologue function at a lower rate than normal gametes.Key words: wheat, Triticum, Elytrigia elongata, alien chromosome addition lines.


1983 ◽  
Vol 41 (2) ◽  
pp. 181-202 ◽  
Author(s):  
Gary E. Hart ◽  
Neal A. Tuleen

SUMMARYThe zymogram phenotypes of 11 enzymes were determined for 22 Triticum aestivum cv. Chinese Spring-Elytrigia elongata disomic and ditelosomic chromosome addition lines. Eleven isozyme structural genes were located in specific arms of six E. elongata chromosomes, as follows: Gpi-E1 in 1ES, Est-E1 in 3ES, Got-E3 in 3EL, Adh-E1 and Lpx-E1 in 4ES, Adh-E2 and Lpx-E2 in 5EL, Amp-E1 in 6Eα, Adh-E3 and Got-E2 in 6Eβ, and Ep-E1 in 7EL. The E. elongata chromosomes present in five disomic addition lines have previously been designated 1E, 2E, 4E, 6E, and 7E to indicate their homoeology with Chinese Spring chromosomes. The results of this study support these designations. The development of disomic putative 3E and 5E addition lines is reported. The added chromosomes designated IV, V, and VI that are present in three of the seven original disomic T. aestivum-E. elongata addition lines are translocated. Evidence that VL and VIL are opposite arms of 2E and that IV is partially homoeologous to 3E has been published. The results reported in this paper indicate that IVS = 3ES, IVL = 7EL, VS = 3ES, and VIS = 5ES and are consistent with VL and VIL being opposite arms of 2E. The synteny relationships of the 11 E. elongata isozyme genes identified in this study are fully consistent with those of homoeologous T. aestivum cv. Chinese Spring genes and thus provide evidence that the gene synteny groups which these two species inherited from their common ancestor are conserved. This study further documents the valuable role that studies of isozyme genes can play in the isolation, characterization, and maintenance of alien chromosomes, telosomes, and chromosomal segments in wheat strains.


Genetics ◽  
1998 ◽  
Vol 149 (4) ◽  
pp. 2025-2037 ◽  
Author(s):  
E V Ananiev ◽  
R L Phillips ◽  
H W Rines

Abstract The recovery of maize (Zea mays L.) chromosome addition lines of oat (Avena sativa L.) from oat × maize crosses enables us to analyze the structure and composition of specific regions, such as knobs, of individual maize chromosomes. A DNA hybridization blot panel of eight individual maize chromosome addition lines revealed that 180-bp repeats found in knobs are present in each of these maize chromosomes, but the copy number varies from ~100 to 25,000. Cosmid clones with knob DNA segments were isolated from a genomic library of an oat-maize chromosome 9 addition line with the help of the 180-bp knob-associated repeated DNA sequence used as a probe. Cloned knob DNA segments revealed a complex organization in which blocks of tandemly arranged 180-bp repeating units are interrupted by insertions of other repeated DNA sequences, mostly represented by individual full size copies of retrotransposable elements. There is an obvious preference for the integration of retrotransposable elements into certain sites (hot spots) of the 180-bp repeat. Sequence microheterogeneity including point mutations and duplications was found in copies of 180-bp repeats. The 180-bp repeats within an array all had the same polarity. Restriction maps constructed for 23 cloned knob DNA fragments revealed the positions of polymorphic sites and sites of integration of insertion elements. Discovery of the interspersion of retrotransposable elements among blocks of tandem repeats in maize and some other organisms suggests that this pattern may be basic to heterochromatin organization for eukaryotes.


1983 ◽  
Vol 42 (2) ◽  
pp. 219-227 ◽  
Author(s):  
C. C. Ainsworth

SUMMARYIn extracts of mature wheat grains, 13 hexokinase isozymes were distinguished by IEF. The genes controlling the production of five isozymes were located on chromosome arms 1BS, 1DS and 3BS by nullisomic analysis. The three loci, part of two homoeoallelic series (Hk-1 and Hk-2) are designated Hk-B1, Hk-D1 and Hk-B2 respectively. Analysis of chromosome 1D short-arm terminal deletions indicated the Hk-D1 locus to be located proximally to the glucose phosphate isomerase locus, Gpi-D1 on the shortarm. Three variant HK phenotypes were distinguished amongst 55 hexaploid wheats examined. Analysis of seven Chinese Spring/Agropyron elongatum chromosome addition lines showed that Ag. elongatum isozymes were expressed in the wheat background in additions IV and V.


1985 ◽  
Vol 45 (2) ◽  
pp. 127-142 ◽  
Author(s):  
Michael E. Pietro ◽  
Gary E. Hart

SummaryThe zymogram phenotypes of triosephosphate isomerase (TPI) were determined for a large number of aneuploid derivatives of Triticum aestivum cv. ‘Chinese Spring’ and for six wheat-alien species chromosome addition series. Examination of the available compensating nullisomic-tetrasomic and homoeologous groups 3 and 5 ditelosomic lines of Chinese Spring disclosed that T. aestivum possesses two systems of dimeric TPI isozymes, designated TPI-1 and TPI-2. The genes TPI-A1, TPI-B1 and TPI-D1 were located in Chinese Spring chromosome arms 3Ap, 3Bp and 3Dp, respectively and the genes TPI-A2, TPI-B2 and TPI-D2 in chromosome arms 5Aq, 5Bq and 5Dq, respectively. TPI-1 genes were also located in Hordeum vulgare cv. Betzes chromosome 3H, T. longissimum chromosome G, Elytrigia elongata chromosome 3E, and Secale cereale cvs. Imperial and Dakold chromosome 3R. TPI-2 genes were found in Betzes chromosome 5H, T. umbellulatum chromosome 5U, T. longissimum chromosome F, and Imperial and Dakold chromosome 5R. These gene locations provide evidence of homoeology between the alien chromosomes in which the genes are located and the chromosomes of homoeologous groups 3 and 5 of Chinese Spring, respectively. Evidence was obtained for the presence of a TPI-R2 gene in each of the T. aestivum cv. Kharkov -S. cereale cv. Dakold chromosome addition lines studied suggesting that this gene is present in the wheat genome in each member of this addition series.


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