Development of a Microsatellite Library for Puccinia coronata Hattie R. Dambroski and Martin Carson, USDA-ARS-Cereal Disease Laboratory, St. Paul, MN Introduction Puccinia coronata or oat crown rust is a devastating disease in wild oats (Avena fatua and A. sterilis) and cultivated oats (A. sativa) in the United States and other parts of the world. P. coronata is highly polymorphic for virulence and avirulence corresponding to resistance genes found originally in A. sterilis and now introgressed into A. sativa cultivars (Leonard, K. J. et al 2004). This polymorphism is found in the Northern Great Plains of the United States where the P. coronata populations are presumably mostly sexual due to the widespread occurrence of the alternate host, buckthorn (Rhamnus cathartica), as well as in the Southern Plains of the United States where the populations are mostly asexual (Leonard, K. J. , 2003). One of the most accepted hypothesis is that of the Puccinia pathway where cereal rust spores (including P. coronata) from the southern plains are blown north later in the season, serving as a significant source of inoculum infecting oats in the northern plains and potentially increasing polymorphism in the north (Simons, M. D. 1970). Our goal was to form a microsatellite library to test the population genetics of this species. P. coronata has no microsatellite (simple sequence repeats, SSR) markers available for use in population studies and microsatellite markers from P. graminis, wheat stem rust, and P. triticina, wheat leaf rust were tried in P. coronata, with no success. Materials and Methods Reactions were run in a thermal cycler (MJ Research Model PTC-100) using the program: Linker Connection Initial Denaturation 25 Cycles Final Amplification 72ºC 94ºC 68ºC 72ºC 5 min 3 min 1 min 2 min 10 min The fragments were checked on an agarose gel. Amplified fragments were enriched using Dynabeads® M-280 Streptavidin (Dynal Biotech, Lake Success, NY) • 15 µl of amplified fragments were denatured for 10 mins at 98°C and then chilled on ice for two min • The probe mixture (4 µl of biotinylated (CA)15 oligonucleotide [0. 125 µg/µl] and 19 µl of 2 X hybridization buffer (1 M sodium phosphate, p. H 7. 4, 1% SDS, 1% BSA)) was added to the fragments after the denaturation and allowed to hybridize overnight. • At room temperature (RT) Dynabeads were washed in 1 X TBST buffer (0. 1 M Tris Base, p. H 7. 5, 150 m. M Na. Cl, 0. 1% Tween 20) three times before being used. • Then the hybridized probe solution was added to the beads and remained at RT for 15 mins, for biotin to bind to streptavidin. • The beads were again washed three times with 1 X TBST and then sterile water was added and the beads were incubated at 98ºC for 10 mins to cleave the biotin from the streptavidin. Germinated urediniospores of P. coronata (isolate CDL 03 MN 097) was ground by shaking samples with 1 mm glass beads (Lysing Matrix C, Q Bio Gene, Irvine, CA) and 25 mg of diatomaceous earth for 20 s. DNA was extracted from this ground mixture using the Omni-Prep DNA Using the supernatant from above, a 50 µl PCR reaction was set up with the extraction kit (Genotech, St. Louis, MO). The microsatellite library was final concentration made using the protocol from the Molecular Markers: Tools for Developing Enriched Microsatellite Libraries Workshop given by Ginger 1 X PCR buffer Clark and Daniel Brazeau at the Interdisciplinary Center for Biotechnology 1. 5 m. M Mg. Cl 2 Research, University of Florida, May 2005. 100 µl each d. NTP • DNA was digested with the restriction enzyme, Sau 3 A I. • Fragments were selected for those size 400 bp and bigger using a Chroma Spin + TE 400 column (Clontech Laboratories, Inc, Palo Alto, CA) and checked on an agarose gel. • Sau 3 A I linkers were ligated to the selected fragments overnight and the excess linkers were removed using the Chroma Spin column. • Linker ligated DNA was amplified in 100 µl reactions with a final concentration of: 1 X PCR buffer 1. 5 m. M Mg. Cl 2 2 m. M each d. NTP 0. 5 µM Sau 3 A I primer 2. 5 U of Taq polymerase 15 µl of linker ligated DNA (about 150 ng) 0. 5 µl Sau 3 A I primer For the final three libraries an additional selection step of a colony lift hybridization was added after cloning. • A nylon membrane was placed on the surface of each plate and allowed to sit at RT for 5 mins and then the membrane spent 5 mins on each of the solution absorbed 3 mm filter paper in the following order: Ø (1) 10% SDS Ø (2) and (3) Denaturing solution (0. 5 M Na. OH, 1. 5 Na. Cl) Ø (4) Neutralizing solution (0. 5 Tris, p. H 7. 4, 1. 5 M Na. Cl) Ø (5) 2 X SSC (20 X SSC = 3 M Na. Cl, 0. 3 M Na citrate, p. H 7. 0). • The DNA was cross-linked by placing DNA side of membrane down on a UV box for 5 mins. • The membrane was then treated with a prehybridization solution (6 X SSC, 5 X Denhardts, 0. 5% SDS for a total of 10 ml) for 30 mins at 55°C. • The prehybridization solution was poured off and the membrane was treated with a hybridization solution (6 X SSC, 0. 5% SDS and 50 ng biotin labeled repeat probe for a total of 10 ml) for one hour at 55°C. • The membrane washed two times at RT for 5 mins with 1 X SSC, 0. 1% SDS for a total of 25 ml. • Next it washed two times at 55°C for 5 mins with 0. 1 X SSC, 0. 1% SDS for a total of 25 ml. • Finally it washed briefly in 10 ml of 2 X SSC. • Hybridization for chemiluminescent detection of the repeats was done using the Phototope® - Star Chemiluminescent Detection Kit (New England Biolads, Inc, Ipswich, MA). Results The first CA library had a success rate of only two polymorphic markers out of 192 sequenced clones. Three more libraries were constructed with enrichment of repeats AAT, AAC and CA. An additional selection of hybridization with biotin-labeled probes was used on these libraries to reduce the number of false positives. No markers were found in the AAT (0/56) or AAC (0/65) libraries, but three markers were found from 45 sequenced clones in the second CA library. These three markers were not polymorphic. The two markers that did work had repeats of (GC)4 and (CA)10 (CT)6. 2. 5 U / 50 µl Taq polymerase 10 µl eluted DNA fragments Reactions were run in a thermal cycler (MJ Research Model PTC-100) using the program: Initial Denaturation 25 cycles Final Amplification 94ºC 3 min 94°C 68°C 72°C 1 min 2 min 10 min • Reactions were checked on an agarose gel. • Cloning was done using Invitrogen’s TOPO TA Cloning Kit. • Sequencing was done at the University of Washington’s High-Throughput Genomics Unit, Seattle, WA. Discussion These libraries did not provide enough markers in order to run any sort of population analysis. We have since contracted with ATG Genetics in Vancouver, BC, Canada to make a library for us and we are currently waiting for that to be completed. The protocol worked for a number of plant and animal species at the workshop, so why these P. coronata libraries did not work is uncertain. It could be that more tinkering needs to be done with the protocol itself in order for it to work on P. coronata. Literature Cited Leonard, K. J. 2003. Regional frequencies of virulence in oat crown rust in the United States from 1990 through 2000. Plant Dis. 87: 1301 -1310. Leonard, K. J. , Anikster, Y. , and Manisterski, J. 2004. Patterns of virulence in natural populations of Puccinia coronata on wild oat in Israel and in agricultural populations on cultivated oat in the United States. Phytopathology 94: 505 -514. Simons, M. D. 1970. Crown rust of oats. Am. Phytopathol. Soc. Monogr No. 5. Heffernan Press, Worcester, MA.
Скачать презентацию Development of a Microsatellite Library for Puccinia coronata
1628b79c0c37f5642d197cf270aa49fd.ppt