Planta Med 2010; 76 - P034
DOI: 10.1055/s-0030-1264332

The first report of microsatellite primer pairs for genetic studies in jojoba [Simmondsia chinensis (Link) Schneider

AG Ince 1, M Karaca 2, AN Onus 1
  • 1Akdeniz University Faculty of Agriculture, Department of Horticulture, Akdeniz University Faculty of Agriculture, Department of Horticulture, 07059 Antalya, Turkey
  • 2Akdeniz University Faculty of Agriculture, Department of Field Crops, Akdeniz University Faculty of Agriculture, Department of Field Crops, 07059 Antalya, Turkey

Jojoba [Simmondsia chinensis (Link) Schneider] is an important industrial plant, native to Arizona, southern California and northern Mexico. The product of primary interest in jojoba is the seed oil, which consists of esters formed from acids and alcohols with chain lengths of 20 or 22 carbon atoms. As many as 300 products containing jojoba have appeared in markets in recent years and the use of jojoba products is expected to increase in future [1]. The use of DNA markers in jojoba breeding is limited and the best method for jojoba improvement has been the selection of plants with desirable characteristics. DNA markers have been extensively used in plant improvement studies [2,3,4]. In the present study a total of 10 microsatellite markers were identified using a strategy described in [5] and this is the first report on jojoba microsatellite markers. In order to evaluate microsatellite primer pairs (Table 1), genomic DNAs of several jojoba samples were extracted using a DNA extraction protocol described in [6]. Results indicated that these primer pairs are very useful in genetic studies of jojoba.

Table 1: List of microsatellite primer pairs and related information

Locus

Forward Primer (5→ 3′)

Reverse Primer (5′→ 3′)

Motif

Size (bp)

JMA01

ACACCAGATTCCAGAGGCATA

ATTCGTCAAAGGGGATGATG

[CT]8

198

JMA02

AGAGTACGCGGGAAGCAGT

TGCTGGCAAGGGAGGTAATA

[AG]8

600

JMA03

AGTCGTTTCCCCTGCTTTTC

CTTCTGCTTATCCCCCTCATC

[CT]7

320

JMA04

GGACCTCTGCCCTTCTTCTT

TGGCGTCTTCACTGCTACTC

[GT]11

500

JMA05

CGGGGATTTATAGTCTTCACTCTC

GTCCAGGCTTCAGACCAGAG

[TC]13

214

JMA06

GCATCTGCCATTTTATGTTCAG

AACCCAGTTCCAGCTTCATC

[AAT]5

180

JMA07

GCCAAGTGGGGATGTAGAGA

GGGGACTGAACTCCACCAA

[GA]8

165

JMA08

GGAACCACAATGGCAACG

CGCAGGAAGGTCGTAAACTG

[TCT]9

185

JMA09

GCGGGGAAAGTGTTACGC

GATTAGCAGAGAAACCAAGGGACT

[AG]15

190

JMA10

AGTCAGAGTCACAGAGCAATGAA

AAGAGATTAGCAGAGAAACCAAGG

[TCT]5

700

References: 1. Ince, A.G. et al. (2009) Genet. Resour. Crop. Ev. doi: 10.1007/s10722–009–9516–1.

2. Karaca, M., Ince, A.G. (2008)J. Genet. 87:83–86.

3. Ince, A.G. et al. (2009) Genet. Resour. Crop. Ev. 56:211–221.

4. Ince, A.G., Karaca, M. (2009)J. Sci. Food Agric. 89:168–176.

5. Ince, A.G. et al. (2008) Plant Cell Tissue Organ Cult. 94:281–290.

6. Karaca, M. et al. (2005) Anal. Biochem. 343:353–355.