Faisal Saeed Awan

A modified mini-prep method for economical and rapid extraction of genomic DNA in plants

Molecular markers for map-based cloning, marker-assisted selection in crop breeding, and genetic studies require DNA isolation from a large number of plants in a short span of time. Here we describe a modified DNA extraction method that is economical in terms of cost, time and labour. The method allows DNA extraction from as little as 0.2–0.3 g of leaves that are homogenized in zipper plastic bags, followed by DNA isolation in 1.5-mL Eppendorf tubes. By using the modified method, a DNA yield of 700–800 μg/300 mg leaf tissue was obtained from cotton and wheat samples. The quality of the DNA was quite suitable for PCR-based markers.

Biodiversity in the sorghum (Sorghum bicolor L. Moench) germplasm of Pakistan.

Sorghum ranks fifth in worldwide economic importance among cereal crops and is one of the most important summer annual grasses of Pakistan. As it is a very diverse crop, sorghum genetic fingerprinting requires an efficient marker system. We estimated genetic divergence among 29 sorghum (Sorghum bicolor) genotypes, including approved varieties and local and exotic lines collected from different ecological regions of Pakistan, using random amplified polymorphic DNA (RAPD) markers. A total of 125 RAPD loci, with an average of 66 loci per genotype, were used to calculate genetic divergence among these genotypes, of which 119 were polymorphic, showing 95% overall polymorphism. Genetic similarity ranged from 0.36 to 0.92, indicating a relatively broad genetic base. RAPD analysis revealed maximum similarity between the Indian III and K-A-113 sorghum genotypes (both exotic lines), while the F-601 and F-606 were observed to be the most diverse genotypes. Mean band frequency revealed by these RAPD primers ranged from 0.17 to 0.56, with an average of 0.36. The data presented here support the findings that RAPDs can be effectively used for studying genetic diversity in sorghum.

Development of a species-specific sequence-characterized amplified region marker for roses.

DNA fingerprints of four rose species, Rosa centifolia, R. Gruss-an-Teplitz, R. bourboniana, and R. damascena, were developed using RAPD-PCR. We identified a unique polymorphic band in R. centifolia. This 762-bp fragment was produced by the random primer GLI-2. The fragment was eluted and directly cloned in a TA cloning vector, pTZ57R/T. Digestion of the plasmid with EcoRI confirmed the cloning of GLI-2(762) in pTZ57R/T. A second enzyme, PstI, used in combination with EcoRI, gave complete digestion of the plasmid, and the 762-bp fragment was confirmed on the gel. Subsequently, the polymorphic amplicon was sequenced with an AB1 373 DNA sequencer system using the PRISM(TM) Ready Reaction DyeDeoxy(TM) Terminator Cycle Sequencing kit. After sequencing, specific primers (23 bp long) were designed based on the sequence of the flanking regions of the original RAPD fragment. These primers will effectively allow fingerprinting for the identification of R. centifolia species. In essence, we developed an SCAR marker to authenticate the identity of R. centifolia species and to distinguish it from its substitutes. Such techniques are required not only to complement conventional parameters in creating the passport data of commercial and medicinal products of rose, but also for routine quality control in commercial and government rosaries and rose nurseries.

Identification and authentication of Rosa species through development of species-specific SCAR marker(s).

Roses (Rosa indica) belong to one of the most crucial groups of plants in the floriculture industry. Rosa species have special fragrances of interest to the perfume and pharmaceutical industries. The genetic diversity of plants based on morphological characteristics is difficult to measure under natural conditions due to the influence of environmental factors, which is why a reliable fingerprinting method was developed to overcome this problem. The development of molecular markers will enable the identification of Rosa species. In the present study, randomly amplified polymorphic DNA (RAPD) analysis was done on four Rosa species, Rosa gruss-an-teplitz (Surkha), Rosa bourboniana, Rosa centifolia, and Rosa damascena. A polymorphic RAPD fragment of 391 bp was detected in R. bourboniana, which was cloned, purified, sequenced, and used to design a pair of species-specific sequence-characterized amplified region (SCAR) primers (forward and reverse). These SCAR primers were used to amplify the specific regions of the rose genome. These PCR amplifications with specific primers are less sensitive to reaction conditions, and due to their high reproducibility, these species-specific SCAR primers can be used for marker-assisted selection and identification of Rosa species.

Genetic diversity in Indian sub-continental landrace cultivars of the genus Triticum L.

Narrowing genetic diversity is a limiting factor in wheat breeding. Popularity of semi dwarf cultivars, developed after green revolution, has resulted in genetic erosion as they replaced indigenous cultivars derived from landraces. These old cultivars have a wealth of useful genes that can be incorporated in the modern cultivars to improve their tolerance level against biotic and abiotic stresses. Genetic analysis of these indigenous and advanced cultivars by the SSR markers has shown greater diversity in this valuable Indian sub-continental germplasm and grouped them into seven units. The Triticum durum lines T2 and T3 were placed in group A, whereas their counterpart T1 was quite distinct. Of the selections, T4 to T9 that was clustered in Group B, T4 to T7 were of Triticum sphaerococcum , whereas the other two were of Triticum aestivum type. T. aestivum cultivar C-248 also appeared to be distinct and could not be grouped with any other cultivar. Based on genetic divergence, therefore, T1 can be used for enhancing diversity in T. durum and C-248 in T. aestivum . Keywords: Triticum , germplasm, simple sequence repeats, genetic diversity

Assessment of biodiversity based on morphological characteristics and RAPD markers among genotypes of wild rose species

Conservation and utilization of the native plant resources is essential for long term sustainability of biodiversity. Wild native resources are adapted to specific and diverse environmental conditions and therefore, these adaptive features can be introduced into modern cultivars either through conventional breeding or advanced molecular genetic techniques. Understanding the genetic make up of the wildly growing plant species and of target desirable genes is a prerequisite for this purpose. Five wild rose ( Rosa L.) genotypes were collected from different locations in northern hilly areas of Pakistan for this study. Different morphological characteristics and PCR based random amplified polymorphic DNA (RAPD) technique was used to find out the diversity and relationship among the genotypes. On morphological basis, Rosa webbiana collected from Muree and Nathia gali showed maximum (83%) similarity, whereas on DNA pattern basis, Rosa brunonii collected from Bansra gali and Sunny bank showed maximum (72%) similarity, while R. webbiana showed maximum diversity among all the species.

Estimation of genetic distance between 10 maize accessions with varying response to different levels of soil moisture

Ten maize accessions (NC-9, A50-2, M-14, B-42, NC-3, T-7, N-48-1, B-34, USSR, and WFTMS) were studied to estimate the genetic distance on molecular level by random amplified polymorphic DNA. These accessions were selected on the basis of their variable responses against different levels of moisture. Twenty-five primers were used to test genetic diversity, of which 14 were observed to be polymorphic. Ninety-three loci were amplified; among these, 77 showed polymorphism and the other 16 were monomorphic. Primers A-13 and C-02 gave the most polymorphic bands, while primers A-01 and C-06 gave the fewest polymorphic bands. The genetic similarities of the 10 maize accessions ranged from 82.8 to 54.8%. Accessions USSR and WFTMS showed greatest similarity, and accessions M-14 and B-42 were found more dissimilar than the other accessions. On the basis of cluster analysis, these 10 accessions were classified in two major groups, A and B, and than further divided into sub-groups. The cluster analysis showed that accessions in the same group as well as in the sub-groups were similar in their physical and morphological characters, since the characters are controlled genetically.

An insight in the genetic control and interrelationship of some quality traits in Brassica napus

A study on three leading lines (KN-256, KN-257, and KN-258) of Brassica napus and an approved variety, Punjab-Sarson, was conducted to gain insight into the genetic control of some quality traits using generation mean analysis. Our results showed that additive gene action predominated in the inheritance of oil content and erucic acid in cross KN-256 x KN-257 and in that of glucosinolates in KN-258 x Punjab-Sarson, indicating that these traits may be improved through selection in early segregating generations. Negative dominance can be exploited through heterosis breeding for the development of lines with low glucosinolates in cross KN-256 x KN-257. Protein content and oleic acid in cross KN-256 x KN-257, and oil content, protein content, and erucic acid in cross KN-258 x Punjab-Sarson depicted non-additive gene action and require further improvement in the later segregating generations. Most of the traits displayed high heritability estimates; glucosinolate content in both the crosses and erucic acid in cross KN- 258 x Punjab-Sarson also displayed high genetic advance, reflecting improvement of the trait in the early segregating generations. All the quality traits were positively correlated with oil content and with one another at both (genotypic and phenotypic) levels in KN-256 x KN-257. Negative correlation was observed between glucosinolate and erucic acid, oleic acid and erucic acid, and linolenic acid and oil content in cross KN-258 x Punjab-Sarson. Thus, gene action changed with the material, and cross KN-258 x Punjab-Sarson carried favorable combinations compared to KN-256 x KN-257.

Morpho-genetic profiling and phylogenetic relationship of guava (Psidium guajava l.) as genetic resources in Pakistan

Guava (Psidium guajava L.) is an open-pollinated crop having 25-40% dissimilarity index which promotes heterozygosity and adds new cultivars. Morpho-genetic characterization of 37 guava accessions was carried out for genetic variability and structure of guava germplasm located in Punjab province, Pakistan. Principal Component analysis (PCA) was subjected to analyze the morphological diversity and for genetic analysis we applied cluster analysis, using the PyElph software. PCA distributed thirty one traits into six components and first two components accounted 39.5% of total variation. A dendrogram constructed on the basis of morphological traits which showed 34% dissimilarity index among thirty seven guava accessions and divided them into 6 groups. For genetic characterization 18 microsatellites were used, the size of reproducible and scorable bands ranged from 150 to 320 bp. The 18 primer pairs amplified 85 alleles with an average number of 4.7 alleles per locus and no more than two displayed bands (nuclear SSR loci). The phylogenetic tree based on molecular analysis showed 50% dissimilarity index among selected guava accessions and separated them into 4 groups.

Gender Identification in Date Palm Using Molecular Markers

Breeding of date palm is complicated because of its long life cycle and heterozygous nature. Sexual propagation of date palm does not produce true-to-type plants. Sex of date palms cannot be identified until the first flowering stage. Molecular markers such as random amplified polymorphic DNA (RAPD), sequence-characterized amplified regions (SCAR), and simple sequence repeats (SSR) have successfully been used to identify the sex-linked loci in the plant genome and to isolate the corresponding genes. This chapter highlights the use of three molecular markers including RAPD, SCAR, and SSR to identify the gender of date palm seedlings.