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Musa Genomics Home > Genome resources > Genomic DNA

Genomic DNA Samples From Reference Accessions list

The DNA comes from a 'mini-core' collection developed in the framework of the Generation Challenge Programme (GCP). The collection currently comprises 52 Musa accessions taken from the Cirad collection located in Guadeloupe (west indies). It was assembled using the GCP criteria regarding the genetic diversity representation, the duplication at the Bioversity International Transit Centre (ITC), the use in breeding programmes and the FAO designation. 

For each of the accessions, ten extractions, each of three grams of frozen leaves were made with the Matab method (Risterucci et al., 2000). About 1 miligram of DNA was obtained per accession. The DNA samples are stored and distributed in PCR grade water.

The DNA samples are distributed to Musa research community via the Musa Genome Resource Centre (MGRC) based at IEB, Olomouc, Czech Republic upon request. The MGRC operates at a cost-recovery basis and the recipients are expected to cover packing and shipment costs. In order to have sufficient researchers benefiting from this service, a maximum of 1 μg of DNA per accession is provided and only under this agreement.

Warning: Until we are able to provide the definitive fingerprinting profile, we cannot guarantee the identity of the DNA sample.

 

Sample
Number

Codes

Name

Section

Species
/Group

Sub-species
/Sub-group

Country of collect

Availability

1

ITC0582

Lady Finger

Eumusa

AAB

India

Yes

2

ITC0649

Foconah

Eumusa

AAB

Pome / Prata

Cameroon

Yes

3

ITC0962

Prata Ana

Eumusa

AAB

Pome / Prata

Brazil

Yes

4

KUWU

Pisang Klutuk Wulung

Eumusa

balbisiana

type 4

Indonesia
(IDN 056)

Yes

5

ITC1156

Pisang Batu

Eumusa

balbisiana

type 4

Indonesia
(IDN 080)

Yes

6

ITC0623

Banksii

Eumusa

acuminata

banksii

Papua New Guinea

Yes

7

ITC0253

Borneo

Eumusa

acuminata

microcarpa

Malaysia, S/E Borneo

Yes

8

ITC0249

Calcutta 4

Eumusa

acuminata

burmannicoides

India

Yes

9

ITC0652

Kluai Tiparot

Eumusa

ABB

Klue teparod

Thailand (THA 020)

Yes

10

ITC1325

Orishele

Eumusa

AAB

Plantain

Nigeria

Yes

11

ITC0472

Pelipita

Eumusa

ABB

Pelipita

Philippines

Yes

12

ITC0767

Dole

Eumusa

ABB

Bluggoe

Yes

13

GRN

Grande Naine

Eumusa

AAA

Cavendish

Guadeloupe

Yes

14

ITC0420

Pisang Kayu

Eumusa

AAA

Orotav

Indonesia
(IDN 098)

Yes

15

ITC1028

Agutay

Eumusa

acuminata

errans

Philippines

Yes

16

ITC0660

Khae (Phrae)

Eumusa

acuminata

siamea

Thailand
(THA 015)

Yes

17

ITC0769

Figue Pomme Geante

Eumusa

AAB

Silk

Guadeloupe

Yes

18

ITC1138

Saba

Eumusa

ABB

Saba

Philippines

Yes

19

ITC1064

Pisang bakar

Eumusa

AAA

Ambon

Indonesia
(IDN 106)

Yes

20

ITC1483

Monthan

Eumusa

ABB

Monthan

India

Yes

21

ITC1120

Tani

Eumusa

balbisiana

Yes

22

ITC0283

Long Tavoy

Eumusa

acuminata

burmannica

Yes

23

ITC0245

Safet Velchi

Eumusa

AB cv

India

Yes

24

ITC0654

Petite Naine

Eumusa

AAA

Cavendish

Yes

25

ITC0766

Paliama

Eumusa

Acuminata

banksii

Papua New Guinea (PNG 067)

Yes

26

ITC1482

Poyo

Eumusa

AAA

Cavendish

Nigeria

Yes

27

ITC0335

Popoulou

Eumusa

AAB

Popoulou/Maia Maoli

Cameroon

Yes

28

SRDJ

Simili Radjah

Eumusa

ABB

Peyan

From India through DRC

Yes

29

ITC1481

Gros Michel

Eumusa

AAA

Gros Michel

Guadeloupe

Yes

30

ITC1152

Wompa

Eumusa

AS

Papua New Guinea (PNG 063)

Yes

31

ITC1034

Kunnan

Eumusa

AB cv

India, Kerala

Yes

32

ITC0312

Pisang Jari Buaya

Eumusa

AA cv (18)

Pisang jari buaya

Malaysia, kelatan Thai border

Yes

33

ITC0653

Pisang Mas

Eumusa

AA cv (2)

Sucrier

Malaysia

Yes

34

ITC0843

Pisang Raja Bulu

Eumusa

AAB

Pisang raja

Indonesia
(IND 093)

Yes

35

ITC0277

Leite

Eumusa

AAA

Rio

Yes

36

ITC0020

Ice Cream

Eumusa

ABB

Ney Mannan

Yes

37

ITC1177

Zebrina

Eumusa

acuminata

zebrina

Indonesia

Yes

38

ITC1187

Tomolo

Eumusa

AA cv

Cooking AA

Papua New Guinea (PNG023)

Yes

39

ITC0247

Honduras

Eumusa

balbisiana

type 1

Honduras (seeds)

Yes

40

BVEL

Lal Velchi

Eumusa

balbisiana

type 3

India

Yes

41

ITC0659

Namwa Khom

Eumusa

ABB

Pisang Awak

Thailand
(THA 011)

Yes

42

ITC0084

Mbwazirume

Eumusa

AAA

Lujugira/Mutika

Burundi

Yes

43

ITC0082

Intokatoke

Eumusa

AAA

Lujugira/Mutika

Burundi

Yes

44

ITC1123

Yangambi km5

Eumusa

AAA

Ibota

DRC

Yes

45

ITC1140

Red Yade

Eumusa

AAB

Plantain

Cameroon

Yes

46

ITC0243

Pisang Rajah

Eumusa

AAB

Nendra padaththi

Malaysia

Yes

47

ITC1238

Yawa 2

Eumusa x Australismusa

ABBT

ABBT Ssp/sgr 501

Papua New Guinea (PNG 072)

Yes

48

ITC1441

Pisang Ceylan

Eumusa

AAB

Mysore

Malaysia

Yes

49

ITC0856

Schizocarpa

Eumusa

schizocarpa

Papua new Guinea

Yes

50

ITC1072

Textilis

Australimusa

textilis

Yes

51

ITC0637

Musa ornata

Rhodochlamys

Ornata

Ornata

Yes

52

ITC1511

DH Pahang (Cirad930)

Eumusa

acuminata

malaccensis

Guadeloupe

Yes

22 SSR markers enabling distinction between the 52 reference accessions

Name

Motifs

Forward sequences (5'-3')

Reverse sequences (3'-5')

T

size
(bp)

Alleles

mMaCIR03

(GA)10

TGACCCACGAGAAAAGAAGC
CTCCTCCATAGCCTGACTGC

55

110-138

14

mMaCIR07

(GA)13

AACAACTAGGATGGTAATGTGTGGAA
GATCTGAGGATGGTTCTGTTGGAGTG

53

146-184

18

mMaCIR08

(TC)6N24(TC)7

ACTTATTCCCCCGCACTCAA
ACTCTCGCCCATCTTCATCC

55

252-298

12

mMaCIR13

(GA)16N76(GA)8

TCCCAACCCCTGCAACCACT
ATGACCTGTCGAACATCCTTT

53

270-298

12

mMaCIR39

(CA)5GATA(GA)5

AACACCGTACAGGGAGTCAC
GATACATAAGGCAGTCACATTG

52

310-350

12

mMaCIR40

(GA)13

GGCAGCAACAACATACTACGAC
CATCTTCACCCCCATTCTTTTA

54

149-187

21

mMaCIR45

(TA)4CA(CTCGA)4

TGCTGCCTTCATCGCTACTA
ACCGCACCTCCACCTCCTG

57

253-275

6

mMaCIR152

(CTT)18

CCACCTTTGAGTTCTCTCC
TTTCCCTCTTCGATTCTGT

54

139-175

20

mMaCIR195

(GA)17

GAATCGCCTTAGTCTCACC
TCATGTGCTCCCATCTTT

54

239-295

16

mMaCIR214

(AC)7

CCATTGAGAGATCAACCC
CTATTTGACGTTGGTGGTC

53

96-116

9

Ma1_32

(GA)17AA(GA)
8AA(GA)2

GGAACAGGTGATCAAAGTGTGA
TTGATCATGTGCCGCTACTG

60

227-270

20

Ma3_90

-

GCACGAAGAGGCATCAC
GGCCAAATTTGATGGACT

53

142-176

18

mMaCIR01

GA(20)

CACGACGTTGTAAAACGACTT
AAAGGTGGGTTAGCATTAGG
TTTGATGTCACAATGGTGTTCC

55

238-314

22

mMaCIR150

(CA) X10

CACGACGTTGTAAAACGA
CATGCTGTCATTGCCTTGT
GAATGCTGATACCTCTTTGG

54

257-270

5

mMaCIR164

(AC) X14

CACGACGTTGTAAAACGAC
AAGACAAGTTCCATTGCTTG
GTTCGGGCTTTCGGT

55

255-409

17

mMaCIR196

(TA) X4, (TC) X 17, (TC) X 3

CACGACGTTGTAAAACGA
CGCTCCAAACCTCCCTTT
CGATGCCACACTGGAC

55

168-192

12

mMaCIR231

(TC) X10

CACGACGTTGTAAAACGACG
CAAATAGTCAAGGGAATCA
ACCCAGGTCTATCAGGTCA

55

238-286

19

mMaCIR24

(TC)7

CACGACGTTGTAAAACGACA
TCTTTTCTTATCCTTCTAACG
ATTAGATCACCGAAGAACTC

48

237-297

19

mMaCIR260

(TG) X8

CACGACGTTGTAAAACGAC
GATGTTTGGGCTGTTTCTT
AAGCAGGTCAGATTGTTCC

55

194-230

13

mMaCIR264

(CT) X17

CACGACGTTGTAAAACGAC
AGGAGTGGGAGCCTATTT
CTCCTCGGTCAGTCCTC

53

234-274

23

mMaCIR27

(GA)9

CACGACGTTGTAAAACGACGG
GGAACAGCACGGTCACAT
CCACTCCCCCAACAACACGA

58

231-259

12

mMaCIR307

(CA) X6

CACGACGTTGTAAAACGACAGA
CTTGTATCGCTTGGTAAA
ACGCTGCACCAGTCAA

54

160-172

6

Protocol for DNA amplification and detection

SSR patterns of each individual of the study were analysed following the protocol of Roy et al. (1996) applied with the automated infrared fluorescence technology of a sequencer LICOR IR2 (LICOR, Lincoln, USA). For a given SSR locus, the forward SSR primer was designed with a 5'-end M13 extension (5'-CACGACGTTGTAAAACGAC-3').
The PCR amplification was performed in a 384 wells Eppendorf mastercycler with 10 ng of Musa DNA in a 10µl final volume of buffer (10 mM Tris-HCl (pH 8), 100 mM KCl, 0.05% w/v gelatin, and 2.0 mM MgCl2) containing 0.08 µM of the M13-labelled primer, 0.1 µM of the other primer, 160 µM of dNTP, 1 U of Taq DNA polymerase (Life Technologies, U.S.A.) and 0.06 µM of M13 primer-fluorescent dye IR700 or IR800 (Biolegio, Netherlands).

The PCR programme contain an initial denaturation step at 94°C for 5 min; a touch-down protocol involving initial decrease of annealing temperature by 1 ºC for the first cycles depending on the primer pairs used, and a fixed annealing temperatures for further 35 cycles. In all cases denaturation occurred  at  94°C for 45 s, annealing at lowest TM of primer (between 43 et 52°C) for 60 s, and elongation at 72°C for 60 s. A final elongation step at 72°C for 5 min is added to all the protocols.

In each plate of PCR a Musa standard made with a mix of three Musa accessions (Pisang Jari Buaya, Popoulou/Maia Maoli and Tomolo) is added in order to improve allele sizes determination.
For each run a ladder (range 71-367 bp) is added at the hedges of the gel. IR700 or IR800-labeled PCR products were diluted 8-fold and 5-fold respectively, subjected to electrophoresis in a 6.5% polyacrylamide gel and then sized by the IR fluorescence scanning system of the sequencer.

 

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