IV. MAIZE GENETICS COOPERATION STOCK CENTER
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Maize Genetics Cooperation � Stock Center USDA/ARS/MWA - Soybean/Maize Germplasm, Pathology & Genetics Research Unit & University of Illinois at Urbana/Champaign - Department of Crop Sciences |
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S-123 Turner Hall |
(217) 333-6631 [phone] (217) 333-6064 [fax] [email protected] [e-mail] http://www.uiuc.edu/ph/www/maize [URL] |
3,216 seed samples have been supplied in response
to 290 requests, for 2005. A total of 96 requests were received from 28 foreign
countries. More than 90% of our
requests were received by electronic mail or through our order form on the
World Wide Web. Popular stock
requests include the IBM RIL mapping populations, Hi‑II lines, ig1 lines, transposable element lines, Maize Gene
Discovery Project lines, and Chromatin stocks.
Approximately 10 acres of nursery were grown this summer at the Crop Sciences Research & Education Center located at the University of Illinois. Favorable weather in the early spring allowed the timely planting of our first crossing nursery. However, dry weather set in, and tender young seedlings in our second crossing nursery were devoured by red-winged blackbirds apparently seeking a source of water. Much of our second crossing nursery will have to be replanted next summer. Growing conditions were generally good, but we had to supplement scant rainfall with irrigation during the first part of the summer. Moderate temperatures and low plant stress resulted in a good pollination season.
Special plantings were made of several categories of stocks:
1. In the �Phenotype Only� collection, we have made available an additional 250 stocks in 2005.
2. Plantings were also made from donated stocks from the collections of Alice Barkan (photosynthetic mutants), Ed Coe (bu1, w3, and nec3 alleles), Hugo Dooner (transposed Ac lines), Jerry Kermicle (various r1 alleles), Robert Lambert (defective kernel mutants), Bruce May and Rob Martienssen (mn* mutants from the MTM project), Gerry Neuffer (EMS-induced mutants), Pat Schnable (glossy mutants), Margaret Smith (male sterile cytoplasm lines), Keith Slotkin (Mu killer), and others. We expect to receive additional accessions of stocks from maize geneticists within the upcoming year.
3. We conducted allelism tests of several categories of mutants with similar phenotype or chromosome location. We found additional alleles of inhibitor of r1 aleurone color2 (inr2), pink scutellum1, spotted1, viviparous9, ramosa1 and white14. We plan to test additional members of the viviparous, spotted leaf, and pale green plant mutants. In this manner, we hope to move more stocks from our vast collection of unplaced uncharacterized mutants into the main collection.
4. We further characterized the Fcu system of r1 aleurone color enhancers. We refined the map position of Fcu on the long arm of chromosome 2 through the collection of five point linkage data, and set up crosses to transposon tag Fcu using one of Tom Brutnell�s transposed Ac lines. We are collecting and characterizing additional alleles of Fcu and other r1 aleurone color enhancers.
5. Two acres were devoted to the propagation of the large collection of cytological variants, including A‑A translocation stocks and inversions. In this collection is a series of waxy1‑marked translocations that are used for mapping unplaced mutants. Over the years, pedigree and classification problems arose during the propagation of these stocks. We can now supply good sources proven by linkage tests to include the correct translocated chromosomes. Additional translocation stocks from this series were tested this last year. Results of these tests will be reported in the next issue of the Maize Genetics Cooperation Newsletter. We have received wx1, su1, o2 and y1 marked translocations from W. R. Findley and wx1 marked stocks from Don Robertson. Approximately 30 of these uniquely marked translocation stocks have been added to our collection. Several others will be added as they are increased. Those marked with wx1 are being checked by linkage tests as we did for the main series of waxy1‑marked translocations.
6. Stocks produced from the NSF project "Regulation of Maize Inflorescence Architecture" (see: https://www.fastlane.nsf.gov/servlet/ showaward?award=0110189) were grown this summer. Families that were observed in 2004 to segregate mutations were selected to be increased in the nursery. These increases help to confirm the presence of the mutation and maintain adequate seed stock to fill future requests.
We continue to grow a winter nursery of 0.5 acres at the Illinois Crop Improvement Association�s facilities in Juana D�az, Puerto Rico. We had an excellent winter crop last year, and all indications are that the crop will perform well this year. We plan to continue growing our winter nurseries at this location.
We have received 2,668 additional EMS lines from various inbred backgrounds produced by Dr. Gerry Neuffer (Regulation of Inflorescence Architecture in Maize project). There are sufficient seed for all of these for distribution. In addition to the EMS lines, we have received an additional 21 lines of Functional Genomics of Chromatin project stocks from Karen McGinnis.
We selected 1,620 lines of materials from Dr. Gerry Neuffer�s EMS material that were screened for ear and kernel mutations in the lab, for placement in observation fields on the University of Illinois Crop Science Research facility for observation of seedling and adult plant mutations (during our annual mutant hunt). In addition to these lines, 1,982 lines of MTM material from Dr. Rob Martienssen were also planted this year and observed for phenotype variation. Many visitors from surrounding universities came throughout the summer to walk the fields and search for unique mutations. We plan to have another mutant hunt next summer.
Our IT specialist, Jason Carter, has
completed the second version of our curation tools, and we are currently using
these tools to maintain data for our collection. These tools now input our public stock data directly into
MaizeGDB, to give maize scientists access to up-to-date information about our
collection. It is hoped that these curation tools will provide the foundation
for the development of more advanced curation tool options for MaizeGDB data
curators. Jason has left us to
join the Peace Corps, and Josh Tolbert joined us in December. Next year, we plan to develop even more
custom software to facilitate the search and display of stock pedigree
information, as well as to streamline the process of filling stock requests.
The new greenhouse space in Urbana is almost ready and new seed storage space (which will double our capacity) is presently being designed.
Marty Sachs |
Philip Stinard |
Janet Day Jackson |
Shane Zimmerman |
Jason Carter/Josh Tolbert |
ADDITIONS TO OUR CATALOG OF STOCKS SINCE MNL79
(For a complete list of our stocks, see: http://maizegdb.org/cgi-bin/stockcatalog.cgi)
CHROMOSOME
1 MARKERS
114H ts2-N2491
CHROMOSOME
2 MARKERS
213K w3-N1907
CHROMOSOME
3 MARKERS
304J wlu8-N1906
CHROMOSOME
5 MARKERS
511I a2 ga2-Rhoades
CHROMOSOME
6 MARKERS
608M tdy1-shadow
CHROMOSOME
7 MARKERS
702J bu1
704G gl1-N489B
711H ra1-N408E
CHROMOSOME
9 MARKERS
905J wx1-0601-Alexander
CHROMOSOME
10 MARKERS
X17A R1-sc
X18F g1 R1-st Mst1 o7
CHROMDB
STOCKS
3201-01.1-T-MCG3348.07
3201-23.1 T-MCG4361.13
3201-27.2 T-MCG5104.05
3201-35.2 T-MCG5812.05
3201-36 T-MCG3331.08
3201-36.1 T-MCG3331.09
3201-37 T-MCG4301.5
3201-38 T-MCG4716.03
3201-39 T-MCG5801.14
3201-39.1 T-MCG5801.18
3201-39.2 T-MCG5801.26
3201-40 T-MCG5211.06
3201-40.1 T-MCG5211.12
3201-41 T-MCG6123.15
UNPLACED
GENES
U139I sur1-B90
U140J zn2-4-6(4461)
ALIEN
ADDITION
T940H Tr5
CYTOPLASMIC-STERILE
/ RESTORER
C736BA Ky21 (J)
Restored; cms-J Rf1 Rf2 Rf3 RfC
TOOLKIT
T3212H tac917.12
INVERSION
I143E Inv1f (1S.85;
1L.56)
I144A Inv1g (1S.41;
1L.35)
I144B Inv1h (1L.70;
1L.87)
I144C Inv1l (1S.82;
1L.46)
I144D Inv1m (1S.81;
1L.10)
I243B Inv2h (2L.13;
2L.51)
I243D Inv2e(3718)
(2S.44; 2S.84)
I243E Inv2c (2L.1;
2L.6)
I244A Inv2g (2S.88;
2L.50)
I244B Inv2l (2S.38;
2L.54)
I244C Inv2o (2S.73;
2L.70)
I344B Inv3d (3S.72;
L.42)
I344C Inv3e (3S.46;
L.80)
I443B Inv4c (4S.89;
4L.62)
I443F Inv4h (4L.16;
4L.56)
I443G Inv4i (4L.19;
4L.66)
I443H Inv4j (4L.24;
4L.66)
I444B Inv4l
I543A Inv4e (4L.16;
4L.81)
I543C Inv5b (5S.80;
5L.91)
I543D Inv5d (5S.42;
5L.63)
I543F Inv5f (5S.67;
5L.69)
I643A Inv5h
I643B Inv5i
I643C Inv6b (6S.38;
6L.92)
I843B Inv7b (7S.32;
7L.30)
I843C Inv7e (7S.89;
7L.93)
I843D Inv8b (8L.10;
8L.42)
I843E Inv8c (8S.11;
8S.98)
IX43B Inv9b (9S.05;
9L.87)
IX43C Inv9c (9S.10;
9L.67)
IX43D Inv10a (10S.57;
10L.86)
PHENOTYPE
ONLY
adherent leaf
3610F ad*-N705B
albescent
3611C al*-N2362B
albino seedling
3511A w*-N1126B
anthocyanin
3611F atc*-N2368
3611G atc*-N2486
bleached leaf
3612I blh*-N2381
3612K Blh*-N2472
defective kernel
3703A de*-N940
3705H de*-N1152
3705L de*-N1174B
3706A de*-N1192
dented kernel
3606C dnt*-N1116
dwarf plant
4406O d*-N2363B
4407A d*-N2367A
4407B d*-N2371
4407D d*-N2374
4407G d*-N2480
4407H d*-N2498
etched endosperm
3802B et*-N557
3803M et*-N956A
3804G et*-N1187B
golden plant
6008B g*-PI254852
green striped leaf
4009G gs*-N163B
4010E gs*-N2382
4010F gs*-N2405
gritty leaf
4010I gtl*-N2488
high chlorophyll
fluorescence
4011B hcf*-N1490B
lesion
3908D les*-N1395C
3908O les*-N2333A
3908P les*-N2363A
3909B Les*-N2397
3909C Les*-N2418
3909E les*-N2502
3909F Les*-NA1176
3909G les*-NA467
lethal
3811M ll*-N2469
male sterile
4012C ms*-N2387B
4012J ms*-N2492B
4012K ms*-N2497A
4012L ms*-N2499
many tillers
4209D Tlr*-N2444
miniature kernel
138-22 mn*-MTM4513
138-35 mn*-MTM4746
238-13 mn*-MTM5341
238-25 mn*-MTM5598
238-29 mn*-MTM5622
238-37 mn*-MTM5806
338-03 mn*-MTM5921
338-14 mn*-MTM6355
338-26 mn*-MTM6975
438-16 mn*-MTM12410
438-42 mn*-MTM15916
638-51 mn*-MTM22311
nana plant
4407J na*-N2366
narrow leaf
3911I nl*-N799B
3911M nl*-N2360B
necrotic leaf
4104KA nec*-N1309B
4104T nec*-N2494
6106Q
yg-nec*-92-1260-79
opaque endosperm
3904K o*-N1111A
3905E o*-N1174A
3906G o*-N1297A
pale green plant
4205N pg*-N498
4304I pg*-N2380
4304M pg*-N2406
4305C pgsm*-N2414
pale green seedling
4203F pg*-N277
4304H pg*-N2369
4304J pg*-N2383A
4304K pg*-N2387A
4304N Pg*-N2447
4304O Pg*-N2473
pale midrib
4305E Pm*-N2443
pale pale green leaf
4306C ppg*-N1986
patched leaf
4105I ptc*-N1076B
4105J ptc*-N2352B
pigmy plant
4407K py*-N519
red auricle
5809A rau*-6522
salmon silks
5809A rau*-6522
semidwarf
4408J sdw*-N2391A
4408K sdw*-N2392
small kernel
4002D smk*-N1026A
small plant
4410N smp*-N1324B
4411F smp*-N2372
streaked leaf
3711B stk*-N1115B
striate leaf
3709C sr*-N2395
3709D sr*-N2400
tassel seed
4012U ts*-N2490
torn leaf
4107V trn*-N2370A
tube leaf
3912D tbl*-N1113B
unbranched tassel
4012Q sgsp*-N2412
virescent seedling
4510L v*-N1809
white luteus
seedling
4112A wl*-N938B
white sheath
4210E Ws*-N2454
white stripe leaf
4211O str*-N1111B
wilted plant
4209E wi*-N811A
4209J wi*-N2419
yellow green leaf
4308C Yg*-N1586
4309H yg*-N2492A
4309I yg*-N2493
yellow streak leaf
3812Q ysk*-N2385
3812S ysk*-N2481
yellow stripe leaf
3812G ys*-N634B
3812M ys*-N2361
3812O ys*-N2398
zebra necrotic leaf
3712K zn*-N2399A
3712M zn*-N2497B