Abstract

Quantitative trait loci (QTLs) associated with androgenic responsiveness in triticale were analyzed using a population of 90 DH lines derived from the F1 cross between inbred line ‘Saka 3006’ and cv. ‘Modus’, which was used in a number of earlier studies on molecular mapping in this crop. Using Windows QTL Cartographer and MapQTL 5.0, composite interval mapping (CIM) and association studies (Kruskal–Wallis test; K–W) for five androgenesis parameters (androgenic embryo induction, total regeneration and green plant regeneration ability, and two characteristics describing final androgenesis efficiency) were conducted. For the studied components of androgenic response, CIM detected in total 28 QTLs which were localized on 5 chromosomes from A and R genomes. Effects of all QTLs that were identified at 2.0 or above of the LOD score explained 5.1–21.7 % of the phenotypic variation. Androgenesis induction was associated with seven QTLs (LOD between 2.0 and 5.8) detected on chromosomes 5A, 4R, 5R and 7R, all of them confirmed by K–W test as regions containing the markers significantly linked to the studied trait. What is more, K–W test revealed additional markers on chromosomes: 5A, 2BL, 7B and 5R. Both total and green regeneration ability were controlled by genes localized on chromosome 4A. Some of the QTLs that affected final androgenesis efficiency were identical with those associated with androgenic embryo induction efficiency, suggesting that the observed correlation may be either due to tight linkage or to pleiotropy. Key message Five regions of the triticale genome were indicated as revealing significant marker/trait association. Markers located in these regions are potentially useful for triticale breeding through marker-assisted selection.

Highlights

  • One of the features that distinguishes plants from animals is the fact that the majority of differentiated plant cells do not lose their developmental potentialities and under specific conditions can return to a totipotent embryogenic state

  • The analysis of androgenic responsiveness among studied DH lines showed a great variation in all components of this feature: androgenic structure induction, total plant regeneration and green plant regeneration ability

  • It resulted in almost three times higher final androgenesis efficiency for this genotype in comparison with DH line ‘Saka 3006’ both in respect of total and green regenerants production (12 vs. 4 regenerants per 100 isolated anthers (R/100A) and 2 vs. 6 GR/ 100A)

Read more

Summary

Introduction

One of the features that distinguishes plants from animals is the fact that the majority of differentiated plant cells do not lose their developmental potentialities and under specific conditions can return to a totipotent embryogenic state. One of such processes called ‘microspore embryogenesis’/‘androgenesis’ starts with the reprogramming of male gametophytic cells (microspores). Instead of mature pollen grains, the microspore forms an androgenic structure (AS) that closely resembles a zygotic embryo or can sometimes be similar to callus tissue In both cases ASs can regenerate into haploid (n) plants and after genome doubling—into doubled haploids (DH, 2n). It is possible to apply the selected markers in physical mapping, map-based cloning and isolation of the gene of interest

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call