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## Chilean journal of agricultural research

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*On-line version* ISSN 0718-5839

### Chilean J. Agric. Res. vol.75 no.2 Chillán June 2015

#### http://dx.doi.org/10.4067/S0718-58392015000200003

**RESEARCH**

**A bayesian approach to inferring the genetic population structure of sugarcane accessions from INTA (Argentina)**

**Mariana Inés Pocovi ^{1*}, and Jorge Alberto Mariotti^{1}**

^{1}Universidad Nacional de Salta, Facultad de Ciencias Naturales, Avenida Bolivia 5150, 4400 Salta, Argentina. *Corresponding author (fcn13161@gmail.com).

Understanding the population structure and genetic diversity in sugarcane *(Saccharum officinarum *L.) accessions from INTA germplasm bank (Argentina) will be of great importance for germplasm collection and breeding improvement as it will identify diverse parental combinations to create segregating progenies with maximum genetic variability for further selection. A Bayesian approach, ordination methods (PCoA, Principal Coordinate Analysis) and clustering analysis (UPGMA, Unweighted Pair Group Method with Arithmetic Mean) were applied to this purpose. Sixty three INTA sugarcane hybrids were genotyped for 107 Simple Sequence Repeat (SSR) and 136 Amplified Fragment Length Polymorphism (AFLP) loci. Given the low probability values found with AFLP for individual assignment (4.7%), microsatellites seemed to perform better (54%) for STRUCTURE analysis that revealed the germplasm to exist in five optimum groups with partly corresponding to their origin. However clusters shown high degree of admixture, F_{ST} values confirmed the existence of differences among groups. Dissimilarity coefficients ranged from 0.079 to 0.651. PCoA separated sugarcane in groups that did not agree with those identified by STRUCTURE. The clustering including all genotypes neither showed resemblance to populations find by STRUCTURE, but clustering performed considering only individuals displaying a proportional membership > 0.6 in their primary population obtained with STRUCTURE showed close similarities. The Bayesian method indubitably brought more information on cultivar origins than classical PCoA and hierarchical clustering method.

**Key words: **AFLP, bayesian clustering, hierarchical clustering, principal coordinate analysis, *Saccharum officinarum, *SSR.

**INTRODUCTION**

Accurate assessment of population structure and genetic diversity levels can be invaluable in crop breeding for different applications. It could provide pivotal information for resource management ensuring a diversified germplasm bank that plays a key role in both breeding and genomic research. The study of genetic diversity of germplasm collections, coupled with genetic differentiation estimates, can facilitate reliable classification of accessions, establishment of their pairwise and group genetic relationships, selection of representative samples which capture genetic diversity of the collection, detection of patterns of differentiation in the whole collection as well as in samples drawn from it and, for breeding purposes, can be particularly useful in planning crosses defining parental lines to be used in the development of new materials.

Population structure analysis has been based in principles underlying Wright's F-statistics. While this approach has been broadly used in the analysis of natural populations, its application in the analysis of germplasm banks has been limited (Allcochete et al., 2008). In the past, determination of germplasm collections genetic structure has mainly been done using traditional multivariate statistical methods usually based on agronomic data. In recent years, the incorporation of DNA data increased the effectiveness in exploring diversity and provided accurate estimations of genetic relationships. Clustering analysis and multivariate analysis do not assume predefined structures. However, these graphical methods are only loosely connected to statistical procedures allowing the identification of homogeneous clusters of individuals. In recent years, many new methods have been developed especially for studying structure in natural and germplasm collections using molecular markers. One of these is the alternative model-based method developed by Pritchard et al. (2000) which aims at delineating clusters of individuals on the basis of their genotypes at multiple loci using a bayesian approach (Evanno et al., 2005; Odong et al., 2011).

Sugarcane is one of the most important industrial crops in tropical and subtropical regions and is cultivated in more than 90 countries around the world primarily for its ability to store high concentrations of carbohydrates for the production of sugar and biofuel. National Institute of Agricultural Technology (INTA) administrates the main Sugarcane Germplasm Bank in Argentina and, carries out a breeding program.

With large number of accessions, genebank managers are faced with numerous choices on how best to conserve these resources and make them available to be utilized in breeding procedures. In the last several years, many efforts have been focused on studying sugarcane genetic diversity on the base of molecular data. Most of the works have been based on various clustering methods. Hierarchical clustering outputs binary trees organize these clusters hierarchically, with the hope that this hierarchy agrees with the intuitive organization of real-world data. These hierarchical structures are also a natural representation for data which was not generated by evolutionary processes, as in the case of materials from a collection of germplasm. There is other limitation to this traditional hierarchical clustering algorithm. The algorithm provides no guide to choosing the "correct" number of clusters or the level at which to prune the tree. Bayesian clustering algorithm overcomes these limitations using marginal likelihoods to decide which clusters to merge (Heller, 2007).

The objective of this paper was to analyze by means of amplified fragment length polymorphism (AFLP) and amplification simple sequence repeat (SSRs) data, the population structure and genetic diversity among sugarcane accessions selected from the INTA's Germplasm Bank (Tucumán, Argentina). In addition, we also compared the performance of hierarchical clustering and ordination techniques with model-based clustering methods.

**MATERIALS AND METHODS**

Sixty three sugarcane accessions from the Instituto Nacional de Tecnología Agropecuaria INTA Germplasm Bank (Tucumán, Argentina) were included in this study (Table 1). These genotypes are of interest for breeding purposes in Argentina due to their adaptability to subtropical growing areas (short cycle and early maturity). Some of these materials are or were used as commercial varieties in Argentina and other countries. Total genomic DNA was extracted from young leaves in these materials, according to Doyle and Doyle (1987).

**Table 1. Sugarcane varieties included in the genetic variability analysis and country of origin (CO).**

**SSR amplification and AFLP procedure**

Based on the consistency of band patterns obtained in a previous study, thirteen SSR primers were chosen (Table 2). Polymerase chain reactions (PCRs) were performed according to (Pocovi et al., 2013). Each of the amplifications was repeated at least twice by independent PCR to examine the reproducibility and confirm band patterns.

**Table 2. Simple Sequence Repeat (SSR) primers used for genotyping 63 sugarcane accessions from the INTA Sugarcane Germplasm Bank (Tucumán, Argentina).**

Amplified Fragment Length Polymorphism (AFLP) was carried out according to Pocovi et al. (2008) with 18 primers+3 combinations (M47/P32; M47/P37;M47/P39; M48/P37; M48/P43; M48/P45; M49/P37; M49/P39;M49/ P43; M49/P45; M50/P39; M50/P43; M59/P37; M59/ P39;M59/P43; M62/P32; M62/P43, and M62/P45).

Amplification Simple Sequence Repeat (SSR) and AFLP products were separated on 6% denaturing polyacrylamide gels for 1.5 h at 60 W using a GibcoBRL Model S2 Sequencing Gel Electrophoresis Apparatus (Life Technologies, Paisley, Scotland). The gels were stained with silver nitrate according to Creste et al. (2010). The resulting banding pattern was scored manually as presence (1) or absence (0) of amplified marker.

**Analysis of genetic structure: Bayesian approach and PCoA**

The model-based program STRUCTURE (Pritchard et al., 2000) was used to infer population structure by a bayesian approach using SSR marker dataset and AFLP data. STRUCTURE 2.3.3 (Stanford University, Stanford, California, USA) was run with the admixture model, a burn-in period of 5 000 and 50 000 Markov Chain Monte Carlo. The optimal value of K was identified using the method developed by Evanno et al. (2005). Twenty independent runs were performed for each simulated value of K, ranging from 1 to 10. Subsequently, a Pr(X|K) index with respect to each K was used to calculate ΔK using the formula described by Evanno et al. (2005). The optimal K depends on the highest peak of ΔK = |L"(K)|/s[Pr(xIk)], where (|L"(K)| denotes the absolute value of the second order rate of change of Pr(X|K), and s[Pr(x|k)] the standard deviation of the Pr(X|K)). Therefore, we compared clustering at the optimum K value with those from Principal Coordinate Analysis (PCoA) and classification Unweighted Pair Group Method with Arithmetic Mean (UPGMA), and Ward to look for the best match.

Principal Coordinate Analysis was also carried out based on SSR genetic dissimilarities matrix for examining population structure. Sugarcane accessions were plotted in a bidimensional space using the INFOSTAT vs2013p (Di Rienzo et al., 2013).

**Classification**

Genetic dissimilarities among all possible pairs of sugarcane accessions were calculated from SSR data as *d = sqrt (1 - s _{ij}) *where

*s*corresponds to the Jaccard similarity coefficient. The resulting similarity matrix was subjected to cluster analysis by two different algorithms UPGMA and Ward method that employs ANOVA approach for calculating the distances between clusters. The goodness of fit of the clustering to the data matrix was determined by calculating the cophenetic correlation coefficient between the similarity matrix and the cophenetic matrix, and the reliability of the dendrogram was tested by bootstrap analysis with 100 replicates using DARwin 5.0.158 software (Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD), Paris, France) (Perrier and Jacquemoud-Collet, 2006). For each analysis, the relationships between all pairs of genotypes were visualized as dendrograms.

_{ij}The results from hierarchical cluster analysis were also compared with the results from STRUCTURE with regard to cluster composition and appropriate number of clusters.

**RESULTS AND DISCUSSION**

107 SSR and 136 AFLP loci were utilized to assess genetic population structure and genetic diversity among 63 sugarcane accessions. Figure 1 shows the fingerprint of the 243 loci. The illustration offers a graphic visualization of the variability estimated among the 63 sugarcane genotypes included in the study and provides a unique genetic "bar-code" for each accession.

**Figure 1. Simple Sequence Repeat (SSR) and Amplified Fragment Length Polymorphism (AFLP) fingerprints of sugarcane accessions from INTA (Instituto de Tecnología Agropecuaria, Argentina) Germplasm Bank. Shared absent bands (0) are shown in black; white color indicates shared bands, (1) and grey squares indicate missing data.**

** Sugarcane population structure inferred from SSR data: Bayesian approach**

A large number of methods have been proposed to deal with the optimum number-of-clusters problem. In this paper, the modal value of the ΔK distribution indicated that the true K value or the uppermost level of structure was five (Figure 2a).

**Figure 2. Graphical method for the detection of the true number of K groups using Single Sequence Repeat (SSR) and Amplified Fragment Length Polymorphism (AFLP) data (b). ΔK calculated as ΔK = |L''(K)|/SD. In a the highest peak was identified at K = 5; in b the peak was identified in K = 6.**

Clearly, each of the five optimal clusters has a considerable proportion of mixed memberships sharing among clusters. The bayesian approach can be considered a quantitative clustering method as computes the proportion of the genome of an individual originating from each inferred population. From the total of 63 sugarcane accessions investigated, 34 (54%) have more than 0.60 membership in any given of the five clusters. The remaining 46% (29 accessions) share similar membership coefficients for at least two groups indicating a high degree of admixture. However, the mean value of alpha resulted 0.1772. According to Evanno et al. (2005), when alpha is close to zero, most individuals are essentially from one population or another, while alpha > 1 means that most individuals are admixed. The same concept was proposed by Ostrowski et al. (2006) who indicated that a relatively small value of the alpha parameter indicated that most accessions originated from one primary ancestor, with a few admixed individuals. In our case, few parents have been used at the beginning of the breeding program in the search of adaptability to subtropical climates (short cycle and early maturity). For this reason most sugarcane accessions share common ancestors.

Cluster IV (in yellow) was the group with the largest number of sugarcane accessions (16), but having the higher percentage of accessions with less than 0.60 membership in that given cluster (25%) indicating that these accessions share similar membership coefficients for any given cluster. Clusters I (in red), II (in green), III (in blue) and V (in pink) included 13, 11, 9, and 14 accessions with 46%, 45%, 56%, and 65% with more than 0.6 membership in each given cluster respectively (Figure 3).

**Figure 3. Structure of sugar cane accessions based on Bayesian assignment probabilities. Structure inferred on Single Simple Repeat (SSR) data. Each sugarcane accession is represented by a vertical line, which is partitioned into K colored segments that represent the individuales estimated membership fractions in K cluster (K = 5). Individuals have been sorted by decreasing membership in the cluster with highest assignment probability for that population.**

Mean F_{ST} values confirmed the existence of differences among clusters. Cluster 3 showed the highest FST value (0.63), followed by cluster 5 (0.38) and cluster 1 (0.29). It is generally accepted that F_{ST} values under 0.05 indicate negligible genetic differentiation while those over 0.25 indicate a great deal of genetic differentiation (Zhao et al., 2010).

Although the origin for each individual was not used in the clustering algorithm, the classification of clusters appeared moderately correlated with the origin of sugarcane accessions (Table 1, Figure 3). Twenty nine from the total of genotypes clustered according to their origins, while the remnant showed a partial or predominant membership of populations of other origins. Clusters I, IV, and V grouped 6 (46%), 13 (82%), and 10 (72%) accessions respectively who share their origins in each group (Salta, Louisiana, and Tucumán) (Figure 3). It can be seen that SSR were quite efficient in detecting sugarcane accessions from Louisiana and Tucumán. Relatedness among samples influences the ability of STRUCTURE to correctly detect the genetic stratification of the remaining materials. In this sense, Clusters II included mixed genotypes in relation to its origin and finally, cluster III grouped sugarcane accessions mainly from Tucumán and Salta.

**Sugarcane population structure inferred from AFLP data: Bayesian approach**

The ?K criterion suggested gave the highest value at K = 6 for AFLP data. However, individual assignments revealed that only three accessions (4.7%) have more than 0.60 memberships in any given of the six clusters. In this regard, microsatellites seemed to perform better (54%) than AFLP data set. Differences in assignment percentages between diverse molecular data were also reported by independent studies in various germplasm materials and were attributed to different information content (Emanuelli et al., 2013).

Given the low probability values for individual assignment found with AFLP, the structure analysis was left aside in that case, and only STRUCTURE results based on SSR were compared with PCoA and clustering analyses.

**Sugarcane population structure: PCoA**

The genetic relationship among the 63 sugarcane accessions was assessed by PCoA based on genetic dissimilarities. The first two principal coordinates explained 35% and 11% of the variability respectively. There are several approaches for determining the number of components to interpret from PCoA. According to Cliff (Franco and Hidalgo, 2003), there should be considered acceptable those coordinates whose accumulated values account for 70% or more of the total variance. In our case, the first seven coordinates accounted for 71% of the total variance. It is common that PCoA results are interpreted by simple visual inspection of plots of points along the first two or three axes. Reeves and Richards (2009) noted two main problems in this practice. First, the practice is highly subjective. Patterns can be deceiving, especially when plots are enhanced with additional visual information such as outlines, or when the point marker is varied according to *a priori *ideas of population structure. Second, the first two or three axes normally may explain only a small proportion of the total variation in a data set. More principal coordinate axes would be needed to meet the 70% threshold. Therefore, any method for interpreting ordination analyses of multilocus data should be capable of considering many or all axes simultaneously, and the visual inspection method is inadequate in this respect.

The first principal coordinate (CP1) separated individuals in three groups colored in blue (Figure 4). The second principal coordinate (CP2) separated most sugarcane accessions in other three different groups (in red). In neither case groups agreed with those identified by STRUCTURE. According to Mohammadi and Prasanna (2003), cluster analysis proved to be more sensitive for detecting pedigree relationships among genotypes than PCoA when the first two or three PCos explained < 25% of the total variation.

**Figure 4. Scatter plot of the first and second principal coordinates of the 63 sugarcane accessions. CP1 and CP2 refer to the first and second principal coordinates. The numbers in parentheses refer to the proportion of variance explained by the principal coordinates. Blue and red circles indicate different groups in CP1 and CP2 respectively. Genotype colors (yellow, red, pink and blue) correspond to those assigned by STRUCTURE.**

**Clustering inferred from SSR data**

Histogram of pairwise dissimilarity from the SSR data indicates a normal distribution with a mean of 0.45 (Figure 5). The dissimilarity coefficients ranged from 0.079 to 0.651. The majority of the dissimilarity coefficients were observed between 0.5 and 0.6. The most of the SSR-based pairwise comparisons exhibited genetic dissimilarities higher than 0.43.

**Figure 5. UPGMA dendrogram (Jaccard (sqrt(1 - s))). Tree was constructed with all the genotypes with a minimal 70% of valid data (no missing data) for each unit pair. The colors of the sugarcane accessions correspond to the color assigned according to the population to which it belongs in the STRUCTURE analysis. Numbers indicate the limit of 40% statistical support for the topology at a particular node.**

Sugarcane accessions grouped on the right tail with higher genetic distances should be considered as potential parents when planning crosses in the development of new materials. You et al. (2013) reported that the innovation of parents with higher genetic diversity has showed a positive role in sugarcane breeding programs in China broadening of the genetic basis in sugarcane hybridization.

Initially, the two most popular clustering methods used in the literature for determination of the structure of plant germplasm collections, UPGMA and Ward, were applied for constructing trees. The differences between both hierarchical clustering algorithms lie mainly in how the distances between pairs of OTUs or clusters are defined (Odong et al., 2011). In both analyses, trees were constructed with all the genotypes with a minimal 70% of valid data (no missing data) for each unit pair (Figures 5 and 6, respectively).

**Figure 6. UPGMA dendrogram (Jaccard (sqrt(1 - s))). Tree was constructed by considering only individuals displaying a proportional membership > 0.6 in their primary population obtained with STRUCTURE. The colors of the sugarcane accessions correspond to the color assigned according to the population to which it belongs in the STRUCTURE analysis. Numbers indicate the limit of 40% statistical support for the topology at a particular node.**

Some authors agree that UPGMA produces highly unbalanced clusters, with a main cluster and many small clusters, whereas the Ward method built clusters of similar size. In our case, clear differences were evident within UPGMA and Ward clusters. Cutting of UPGMA tree resulted into three slightly unbalanced clusters, while Ward produced two major balanced clusters (Figure 7). Highest CPCC was obtained using UPGMA algorithm (0.76 vs. 0.49 for Ward), which indicated a good fit between the original pair wise distance among accessions and pair wise distances between accessions predicted constructing the dendrogram. Odong et al. (2011) showed that the cophenetic correlation coefficient is directly related to subgroup differentiation and can thus be used as an indicator of the presence of genetically distinct subgroups in germplasm collections. Given that UPGMA performed better than Ward method, the following discussion refers only to the UPGMA.

**Figure 7. Ward dendrogram (Jaccard (sqrt(1 - s))). Tree was constructed with all the genotypes with a minimal 70% of valid data (no missing data) for each unit pair. The colors of the sugarcane accessions correspond to the color assigned according to the population to which it belongs in the STRUCTURE analysis.**

The clustering by UPGMA including all genotypes showed no resemblance to populations find by STRUCTURE. A second clustering was performed considering only individuals displaying a proportional membership > 0.6 in their primary population obtained with STRUCTURE. While this new UPGMA tree was also unable to identify the optimum number of clusters obtained by STRUCTURE (five), it showed close similarities (Figures 7 and 4a). Although analysis by STRUCTURE showed that five is the optimum number of populations, in Figure 6 it can be seen that cluster I from UPGMA contains 61% of the genotypes included in the red STRUCTURE group (Figure 4a); cluster II included 89% of the accessions of the blue group; cluster III contained accessions clustered in STRUCTURE in both the green and yellow populations (56%) and finally, cluster IV grouped 78.5% of the genotypes in the pink STRUCTURE group.

Including in the analysis only individuals displaying a proportional membership > 0.6 in their primary population also allowed improving bootstrap values, increasing the number of nodes with more than 40% of occurrence, however, few internal branches in the tree were supported by bootstrapping.

**CONCLUSIONS**

The comprehensive molecular characterization of the sugarcane accessions contributes to the knowledge about levels and distribution of genetic diversity in the existing INTA sugarcane germplasm bank. Different softwares and methods used for genetic analysis were suitable for confirming a narrow genetic base of the materials; however, there were differences in the subpopulations obtained depending on methods applied. The relatively low genetic variability can partially be explained by the closeness of the subtropical materials used in the study, according to their proposed genealogies and the breeding procedures applied ("modified recurrent selection").

Comparison of the three methods showed that accessions clustered differently based on the method of analysis STRUCTURE, principal coordinates, classification. The Bayesian method used indubitably brought more information on cultivar origins than classical Principal Coordinate Analysis and hierarchical clustering method. The results provide guidance for future efficient use of sugarcane accession in breeding and germplasm bank management. An increase in the genetic diversity of parental accessions should be helpful to broaden the genetic basis of progenies subjected to selection.

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* Received: 30 September 2014.*

*Accepted: 10 March 2015.*