Identification of a RAPD marker linked to the oat stem rust gene Pg3

ISSN:
1432-2242
Keywords:
Polymerase chain reaction ; Disease resistance loci ; Oat DNA ; RAPD primers ; Rapid DNA extraction
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
Notes:
Summary The feasibility of identifying molecular markers linked to disease resistance genes in oats was investigated utilizing random primers in conjunction with polymerase chain reaction technology. A pair of near-isogenic oat lines were screened for polymorphic DNA fragments linked to the stem rust resistance gene Pg3. Two primers were identified which amplified DNA fragments that were polymorphic between the lines analyzed. One primer (ACOpR-2) was shown to be completely linked to the Pg3 locus; the other primer was not linked to either the ACOpR-2 or the Pg3 loci. This type of analysis, combined with rapid leaf disc DNA extraction techniques, offers an effective means of identifying useful molecular markers and of applying them to plant breeding selection strategies.
Type of Medium:
Electronic Resource
URL:
_version_ 1798295969644675072
autor Penner, G. A.
Chong, J.
Lévesque-Lemay, M.
Molnar, S. J.
Fedak, G.
autorsonst Penner, G. A.
Chong, J.
Lévesque-Lemay, M.
Molnar, S. J.
Fedak, G.
book_url http://dx.doi.org/10.1007/BF00225008
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLM199861951
issn 1432-2242
journal_name Theoretical and applied genetics
materialart 1
notes Summary The feasibility of identifying molecular markers linked to disease resistance genes in oats was investigated utilizing random primers in conjunction with polymerase chain reaction technology. A pair of near-isogenic oat lines were screened for polymorphic DNA fragments linked to the stem rust resistance gene Pg3. Two primers were identified which amplified DNA fragments that were polymorphic between the lines analyzed. One primer (ACOpR-2) was shown to be completely linked to the Pg3 locus; the other primer was not linked to either the ACOpR-2 or the Pg3 loci. This type of analysis, combined with rapid leaf disc DNA extraction techniques, offers an effective means of identifying useful molecular markers and of applying them to plant breeding selection strategies.
package_name Springer
publikationsjahr_anzeige 1993
publikationsjahr_facette 1993
publikationsjahr_intervall 8009:1990-1994
publikationsjahr_sort 1993
publisher Springer
reference 85 (1993), S. 702-705
schlagwort Polymerase chain reaction
Disease resistance loci
Oat DNA
RAPD primers
Rapid DNA extraction
search_space articles
shingle_author_1 Penner, G. A.
Chong, J.
Lévesque-Lemay, M.
Molnar, S. J.
Fedak, G.
shingle_author_2 Penner, G. A.
Chong, J.
Lévesque-Lemay, M.
Molnar, S. J.
Fedak, G.
shingle_author_3 Penner, G. A.
Chong, J.
Lévesque-Lemay, M.
Molnar, S. J.
Fedak, G.
shingle_author_4 Penner, G. A.
Chong, J.
Lévesque-Lemay, M.
Molnar, S. J.
Fedak, G.
shingle_catch_all_1 Penner, G. A.
Chong, J.
Lévesque-Lemay, M.
Molnar, S. J.
Fedak, G.
Identification of a RAPD marker linked to the oat stem rust gene Pg3
Polymerase chain reaction
Disease resistance loci
Oat DNA
RAPD primers
Rapid DNA extraction
Polymerase chain reaction
Disease resistance loci
Oat DNA
RAPD primers
Rapid DNA extraction
Summary The feasibility of identifying molecular markers linked to disease resistance genes in oats was investigated utilizing random primers in conjunction with polymerase chain reaction technology. A pair of near-isogenic oat lines were screened for polymorphic DNA fragments linked to the stem rust resistance gene Pg3. Two primers were identified which amplified DNA fragments that were polymorphic between the lines analyzed. One primer (ACOpR-2) was shown to be completely linked to the Pg3 locus; the other primer was not linked to either the ACOpR-2 or the Pg3 loci. This type of analysis, combined with rapid leaf disc DNA extraction techniques, offers an effective means of identifying useful molecular markers and of applying them to plant breeding selection strategies.
1432-2242
14322242
Springer
shingle_catch_all_2 Penner, G. A.
Chong, J.
Lévesque-Lemay, M.
Molnar, S. J.
Fedak, G.
Identification of a RAPD marker linked to the oat stem rust gene Pg3
Polymerase chain reaction
Disease resistance loci
Oat DNA
RAPD primers
Rapid DNA extraction
Polymerase chain reaction
Disease resistance loci
Oat DNA
RAPD primers
Rapid DNA extraction
Summary The feasibility of identifying molecular markers linked to disease resistance genes in oats was investigated utilizing random primers in conjunction with polymerase chain reaction technology. A pair of near-isogenic oat lines were screened for polymorphic DNA fragments linked to the stem rust resistance gene Pg3. Two primers were identified which amplified DNA fragments that were polymorphic between the lines analyzed. One primer (ACOpR-2) was shown to be completely linked to the Pg3 locus; the other primer was not linked to either the ACOpR-2 or the Pg3 loci. This type of analysis, combined with rapid leaf disc DNA extraction techniques, offers an effective means of identifying useful molecular markers and of applying them to plant breeding selection strategies.
1432-2242
14322242
Springer
shingle_catch_all_3 Penner, G. A.
Chong, J.
Lévesque-Lemay, M.
Molnar, S. J.
Fedak, G.
Identification of a RAPD marker linked to the oat stem rust gene Pg3
Polymerase chain reaction
Disease resistance loci
Oat DNA
RAPD primers
Rapid DNA extraction
Polymerase chain reaction
Disease resistance loci
Oat DNA
RAPD primers
Rapid DNA extraction
Summary The feasibility of identifying molecular markers linked to disease resistance genes in oats was investigated utilizing random primers in conjunction with polymerase chain reaction technology. A pair of near-isogenic oat lines were screened for polymorphic DNA fragments linked to the stem rust resistance gene Pg3. Two primers were identified which amplified DNA fragments that were polymorphic between the lines analyzed. One primer (ACOpR-2) was shown to be completely linked to the Pg3 locus; the other primer was not linked to either the ACOpR-2 or the Pg3 loci. This type of analysis, combined with rapid leaf disc DNA extraction techniques, offers an effective means of identifying useful molecular markers and of applying them to plant breeding selection strategies.
1432-2242
14322242
Springer
shingle_catch_all_4 Penner, G. A.
Chong, J.
Lévesque-Lemay, M.
Molnar, S. J.
Fedak, G.
Identification of a RAPD marker linked to the oat stem rust gene Pg3
Polymerase chain reaction
Disease resistance loci
Oat DNA
RAPD primers
Rapid DNA extraction
Polymerase chain reaction
Disease resistance loci
Oat DNA
RAPD primers
Rapid DNA extraction
Summary The feasibility of identifying molecular markers linked to disease resistance genes in oats was investigated utilizing random primers in conjunction with polymerase chain reaction technology. A pair of near-isogenic oat lines were screened for polymorphic DNA fragments linked to the stem rust resistance gene Pg3. Two primers were identified which amplified DNA fragments that were polymorphic between the lines analyzed. One primer (ACOpR-2) was shown to be completely linked to the Pg3 locus; the other primer was not linked to either the ACOpR-2 or the Pg3 loci. This type of analysis, combined with rapid leaf disc DNA extraction techniques, offers an effective means of identifying useful molecular markers and of applying them to plant breeding selection strategies.
1432-2242
14322242
Springer
shingle_title_1 Identification of a RAPD marker linked to the oat stem rust gene Pg3
shingle_title_2 Identification of a RAPD marker linked to the oat stem rust gene Pg3
shingle_title_3 Identification of a RAPD marker linked to the oat stem rust gene Pg3
shingle_title_4 Identification of a RAPD marker linked to the oat stem rust gene Pg3
sigel_instance_filter dkfz
geomar
wilbert
ipn
albert
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source_archive Springer Online Journal Archives 1860-2000
timestamp 2024-05-06T09:44:38.709Z
titel Identification of a RAPD marker linked to the oat stem rust gene Pg3
titel_suche Identification of a RAPD marker linked to the oat stem rust gene Pg3
topic W
uid nat_lic_papers_NLM199861951