Molecular analysis of genetic variation in trees Caroline Agufa Tree Domestication Course, 17 to 22 November 2003 World Agroforestry Centre
Introduction – Why molecular analysis? Techniques for molecular genetic analysis What does molecular analysis reveal about genetic variation in trees? Molecular genetic variation and the impact of tree cultivation Case Studies of molecular analysis Limitations of molecular analysis Molecular analysis of genetic variation in trees
Introduction: Why molecular analysis? Utility of traditional techniques is limited because –Influenced by environmental factors –The number of characters available are few –Long time for evaluation (trees) Therefore, molecular genetic markers are now often used –These provide information on the underlying diversity and genetic constitution of trees and allow more optimal genetic management strategies to be developed
Techniques for molecular genetic analysis The most commonly applied are isozyme and PCR-based approaches Isozyme analysis –Detection of different allelic forms of the same enzyme by electrophoresis and staining –Inherited in a Mendelian and codominant manner Disadvantage: Need fresh material because relies on enzyme activity
Techniques for molecular genetic analysis II Polymerase Chain Reaction (PCR) analysis –amplified fragment length polymorphism –random amplified polymorphic DNA (RAPD) –restriction fragment length polymorphism-PCR –simple sequence repeats Disadvantage: Expensive RAPD profile Arrows indicate polymorphisms
What does molecular analysis reveal about genetic variation in trees? Genetic variation within tree populations is high Molecular genetic differentiation among populations is generally low (but statistically significant). However, there are exceptions, and under-differentiation of some tropical taxa
Clustering of genetic distances (48 RAPD markers) Prunus africana * Cameroon Madagascar Genetic distance Ethiopia Kenya * Mount Kilum * Ntingue * Mendankwe * Mount Cameroon Uganda Manakambahiny Antsevabe Mantadia
‡ populations established using seeds from Kobujoi area Prunus africana Clustering of genetic distances (41 RAPD markers) Mt Kilum 1 (planted) ONADEF (nursery) Mendankwe (planted) Ntingue 2 (natural) Mt Cameroon (natural) Mt Kilum 2 (natural) Sop (natural) Ntingue 1 (planted) MESG (nursery) Bwindi (Uganda) Kobujoi (natural) Muguga (planted) ‡ Maseno (nursery) ‡ Lepsi-Arsi (Ethiopia) Nyeri 1 (natural) Nyeri 2 (planted) Chuka 2 (natural) Meru (natural) Chuka 1 (nursery) Tigoni (natural) Genetic distance Cameroon Western Kenya Eastern Kenya
Sclerocarya birrea Clustering of genetic distances (80 RAPD markers) 0.12
Sclerocarya birrea Principal component analysis for populations of Sclerocarya birrea based on 80 RAPD markers First principal component (11% of variation) Second principal component (7% of variation) Country Kenya Swaziland Mali Namibia Malawi Zambia Tanzania Botswana Magamba Makadaga, Mialo, Mandimu
Uapaca kirkiana Clustering of genetic distances (132 RAPD markers) B Sumbawamga (Tanzania) L Kapelula (Malawi) D Mbeya (Tanzania) K Luwawa (Malawi) J Litende (Malawi) E Songea (Tanzania) A Mpwapwa (Tanzania) C Iringa (Tanzania) M Furacungo (Mozambique) I Chipata (Zambia) H Kanona (Zambia) F Kasama (Zambia) G Kitwe (Zambia) S Mpanzure (Zimbabwe) R Murewa (Zimbabwe) P Musana (Zimbabwe) N Domboshewa (Zimbabwe) Genetic distance
Uapaca kirkiana Principal component analysis for populations of Uapaca kirkiana based on 132 RAPD markers
Molecular genetic variation and the impact of tree cultivation Levels of genetic variation in cultivated material are generally lower than in wild populations A narrow genetic base in cultivated material can have serious negative implications for sustainable utilisation With the trend to tree populations on-farm, more focus is required on assessing genetic variation in cultivated trees, to devise sustainable on-farm management strategies
Limitations of molecular analysis Molecular markers are by nature ‘neutral’ indicators of underlying genetic variation, rather than linked to any one character trait Molecular markers ought to be used in combination with field evaluation techniques