IV.  MAIZE GENETICS COOPERATION STOCK CENTER

 

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

 

 

 

S-123 Turner Hall
1102 South Goodwin Avenue
Urbana, IL  61801-4730

(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