Advanced search×

Genetic association of crown rust resistance gene Pc68, storage protein loci, and resistance gene analogues in oats.

Genome 54(6):484-97 (2011) PMID 21615301

Segregating F(3) families, derived from a cross between oat cultivar Swan and the putative single gene line PC68, were used to determine the association of seed storage protein loci and resistance gene analogues (RGAs) with the crown rust resistance gene Pc68. SDS-PAGE analysis detected three avenin loci, AveX, AveY, and AveZ, closely linked to Pc68. Their diagnostic alleles are linked in coupling to Pc68 and were also detected in three additional lines carrying Pc68. Another protein locus was linked in repulsion to Pc68. In complementary studies, three wheat RGA clones (W2, W4, and W10) detected restriction fragment length polymorphisms (RFLPs) between homozygous resistant and homozygous susceptible F(3) DNA bulks. Four oat homologues of W2 were cloned and sequenced. RFLPs detected with two of them were mapped using F(3) and F(4) populations. Clone 18 detected a locus, Orga2, linked in repulsion to Pc68. Clone 22 detected several RFLPs including Orga1 (the closest locus to Pc68) and three RGA loci (Orga22-2, Orga22-3, and Orga22-4) loosely linked to Pc68. The diagnostic RFLPs linked in coupling to Pc68 were detected by clone 22 in three additional oat lines carrying Pc68 and have potential utility in investigating and improving crown rust resistance of oat.

DOI: 10.1139/g11-014
Version: za2963e q8zab q8zb2 q8zcb q8zd3 q8ze8 q8zf7 q8zg6

Similar articles you may find interesting…

  1. Risk factors for cardiovascular disease in renal transplant recipients and strategies to minimize risk.

    Transpl Int 23(12):1191-204 (2010) PMID 21059108

    Cardiovascular disease is the leading cause of death following renal transplantation, and renal transplant patients have a greatly increased cardiac risk compared with the general population. Death with a functioning graft caused by cardiovascular disease also represents a substantia...
  2. Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies.

    Am J Med 112(3):183-90 (2002) PMID 11893344

    ROMK, NKCC2, and NCCT mutations usually have uniform clinical presentations, whereas mutations in ClC-Kb occasionally lead to phenotypic overlaps with the NCCT or, less commonly, with the ROMK/NKCC2 cohort. Based on these results, we propose an algorithm for the molecular diagnosis of hypokalemic sa...
  3. [Position of the German Society of Internal Medicine on the "Recommendations for the curriculum of medical education by the Expert Committee...

    Internist (Berl) 35(1):87-9 (1994) PMID 8144325