Ikechukwu O. Agbagwa

The value of morpho-anatomical features in the systematics of Cucurbita L. ( Cucurbitaceae ) species in Nigeria

Comparative studies on the morphology and anatomy of the three species of Cucurbita L. (C. moschata, C. maxima and C. pepo ) in Nigeria were carried out. The morphological features of significance include variations in the number of tendrils, fruit size, shape, nature of fruit stalk, leaf shape and flower colour. Seed-coat anatomy revealed four distinct zones, which varied in thickness and tissue layers. Similarities were observed in the distribution, differentiation and number of layers of cells and tissues in the leaf, petiole and stem sections. There were, however, variations in number of bicollateral vascular bundles in their petiole. While the number is 10 in C. moschata , 14 in C. pepo , it is 16 in C. maxima . Parietal placentation and 15 anther-lobes are reported for these species for the first time. The usefulness of these parameters in the taxonomic delimitation of these species is discussed. Key Words: Cucurbita , morpho-anatomy, placentation, seed-coat, taxonomy, vascular bundles. African Journal of Biotechnology Vo l.3(10) 2004: 541-546

A protocol for high-quality genomic DNA extraction from legumes.

Current DNA extraction protocols, which require liquid nitrogen, lyophilization and considerable infrastructure in terms of instrumentation, often impede the application of biotechnological tools in less researched crops in laboratories in developing countries. We modified and optimized the existing CTAB method for plant genomic DNA extraction by avoiding liquid nitrogen usage and lyophilization. DNA was extracted directly from freshly harvested leaves ground in pre-heated CTAB buffer. Chloroform:isoamyl alcohol (24:1) and RNase treatments followed by single-purification step decontaminated the samples thereby paving way for selective extraction of DNA. High molecular weight DNA yield in the range of 328 to 4776 ng/μL with an average of 1459 ng/μL was obtained from 45 samples of cultivated and wild Cajanus species. With an absorbance ratio at 260 to 280 nm, a range of 1.66 to 2.20, and a mean of 1.85, very low levels of protein and polysaccharide contamination were recorded. Forty samples can be extracted daily at a cost between 1.8 and US

Novel genic microsatellite markers from Cajanus scarabaeoides and their comparative efficiency in revealing genetic diversity in pigeonpea

2.0 per plant sample. This modified method is suitable for most plants especially members of the Leguminosae. Apart from Cajanus, it has been extensively applied in DNA extraction from Cicer and Vigna species.

Epigenetic Pattern on the Human Y Chromosome Is Evolutionarily Conserved.

Paucity of molecular markers is hindering molecular breeding programmes for genetic improvement in pigeonpea, which is considered to be among the richest source of dietary protein in Asia and Africa. At the time of the start of this study, only 156 microsatellite markers were available in pigeonpea (Burns et al. 2001; Odeny et al. 2007, 2009). Recently with the publication of draft genome sequence and deep transcriptome studies, the stage has been set to enrich genomic resources to aid molecular breeding in pigeonpea (Dutta et al. 2011; Singh et al. 2012; Varshney et al. 2012). Genic microsatellites or EST-SSRs (simple sequence repeats) derived from expressed sequence tags (ESTs) are useful because these are inexpensive to develop, represent transcribed genes, and often a putative function can be assigned to them. Compared with genomic sequences, genic SSRs have several advantages as genetic markers. First, if an EST marker is found to be genetically associated with a trait of interest, it may represent the gene affecting the trait directly (Chen et al. 2001; Thiel et al. 2003). Therefore, EST-derived markers can provide opportunities for gene discovery and enhance the role of genetic markers by assaying variation in transcribed and known-function genes. Second, EST-derived

Impact of four-dimensional seismic and production activities on the mangrove systems of the Niger Delta, Nigeria

DNA methylation plays an important role for mammalian development. However, it is unclear whether the DNA methylation pattern is evolutionarily conserved. The Y chromosome serves as a powerful tool for the study of human evolution because it is transferred between males. In this study, based on deep-rooted pedigrees and the latest Y chromosome phylogenetic tree, we performed epigenetic pattern analysis of the Y chromosome from 72 donors. By comparing their respective DNA methylation level, we found that the DNA methylation pattern on the Y chromosome was stable among family members and haplogroups. Interestingly, two haplogroup-specific methylation sites were found, which were both genotype-dependent. Moreover, the African and Asian samples also had similar DNA methylation pattern with a remote divergence time. Our findings indicated that the DNA methylation pattern on the Y chromosome was conservative during human male history.

Using AFLP-RGA markers to assess genetic diversity among pigeon pea (Cajanus cajan) genotypes in relation to major diseases

Reconnaissance survey and laboratory appraisal of the mangrove system in seven communities in the Niger Delta (Nigeria) endangered by seismic and production operations revealed several alterations of soil, sediment, and vegetation. Hydrocarbon content in the range of 0.3–1.1 mg/100 g was extracted within the proximities of spill sources and seismic lines. The prospect area covered by our investigation was characterized by a mixed mangrove forest dominated by Rhizophora racemosa. It was observed that the construction of the seismic lines was responsible for the vegetal disorientation recurrent in the area. The grass, Paspalum vaginatum, and the saltwater fern, Acrostichum aureum, were found at the fringe of most dredge spoils. The characteristic tidal inundation which increases mobility of the substrate, salinity fluctuation, and anoxia may also have contributed, at least in part, to the observed despoliation of some of these species found within the vicinities of the seismic lines and hydrocarbon percolation. Extensive revegetation program is recommended to ensure an effective restoration process of this ecologically fragile zone.

Chromosome number and cytomorphological characterization of a polyploid Abrus

Resistance gene analog (RGA)-anchored amplified fragment length polymorphism (AFLP-RGA) marker system was used in order to evaluate genetic relationships among 22 pigeon pea genotypes with varied responses to Fusarium wilt and sterility mosaic disease. Five AFLP-RGA primer combinations (E-CAG/wlrk-S, M-GTG/wlrk-S, M-GTG/wlrk-AS, E-CAT/S1-INV and E-CAG/wlrk-AS) produced 173 scorable fragments, of which 157 (90.7%) were polymorphic, with an average of 31.4 fragments per primer combination. The polymorphism rates obtained with the five primers were 83.3%, 92.0%, 92.3%, 93.0% and 93.1%, respectively. Mean polymorphic information content (PIC) values ranged from 0.24 (with E-CAT/S1-INV) to 0.30 (with E-CAG/wlrk-AS), whereas resolving power (RP) values varied from 11.06 (with M-GTG/wlrk-S) to 25.51 (with E-CAG/wlrk-AS) and marker index (MI) values ranged from 5.98 (with M-GTG/wlrk-S) to 12.30 (with E-CAG/wlrk-AS). We identified a positive correlation between MI and RP (r2=0.98, p<0.05), stronger that that observed for the comparison between PIC and RP (r2=0.88, p<0.05). That implies that either MI or RP is the best parameter for selecting more informative AFLP-RGA primer combinations. The Jaccard coefficient ranged from 0.07 to 0.72, suggesting a broad genetic base in the genotypes studied. A neighbor-joining tree, based on the unweighted pair group method with arithmetic mean, distinguished cultivated species from wild species. The grouping of resistant genotypes in different clusters would help in the selection of suitable donors for resistance breeding in pigeon pea.

Characterization of Ty1/copia-like retrotransposon families from pigeonpea genome.

Chromosome counts from natural populations of Abrus pulchellus in Nigeria were carried out. Tetraploid (2n = 44) chromosome number was constant in all the samples investigated. The 44 chromosomes fall into three cytomorphological categories: eight metacentric and eight submetacentric pairs, and six acrocentric pairs. The chromosomes are relatively small in length ranging from 0.5 to 1.4�m. The polyploid (tetraploid) cytotype is reported for the first time for this taxon.

Identification, Characterization, and Phylogenetic analysis of Pigeon pea (Cajanus cajan L. Mill sp.) Resistance Gene Analogs using PCR cloning and in silico methods

Retrotransposons contribute significantly to the size, organization, and genetic diversity of their host genomes. To characterize novel retrotransposon families in pigeonpea and develop retrotransposon-based sequence-specific amplification polymorphic markers, in silico homology sequence search was carried out against the whole genome shotgun sequence of pigeonpea variety Asha (ICPL87119). For homology searching, 5 copia-like retro elements belonging to soybean, common bean, mungbean, chickpea, and field pea were used as query sequences. Contigs with at least 80% query coverage and >70% similarity were searched for retroelements using the long terminal repeat finder. A total of 28 copia-like retroelements were identified using this method. Multiple sequence alignment for the reverse transcriptase domain indicated conserved reverse transcriptase domains in all 28 elements compared with other reported elements. Phylogenetic analysis based on reverse transcriptase domains revealed 11 families. The copy number per family ranged from 1 (for B, J, and K family) to 8 (I). The sequence-specific amplification polymorphic marker-based insertion site profiling for one of the retrotransposon families (G) confirmed multiple insertions of this element across the pigeonpea genome. This study showed that our in silico homology search strategy was efficient for identifying and characterizing the Ty1/copia-like retrotransposon. The results of this study are useful for developing retrotransposon-based sequence-specific amplification polymorphic markers for pigeonpea crop improvement.

Floral Biology, Breeding System, and Pollination Ecology of Cucurbita moschata (Duch. ex Lam) Duch. ex Poir. Varieties (Cucurbitaceae) from Parts of the Niger Delta, Nigeria

Pigeon Pea (Cajanus cajan), an important grain legume, is susceptible to Fusarium wilt (FW), sterility mosaic disease (SMD), and Phytophthora blight. Identification of resistance gene analogs (RGAs) is important for development of resistant varieties. In this study, degenerate primers targeting nucleotide binding sites (NBS) of known resistance (R) genes were used to amplify RGAs from two Pigeon Pea genotypes with differing disease resistance profiles. The translated cloned RGAs had high amino acid identity (68–71%) with putative disease resistance proteins in Glycine Max. Five RGA open reading frames were found in the whole Pigeon Pea genome after BLASTN analysis with the cloned sequences. Translated RGA proteins contained several characteristic features such as the NB-ARC domain (characteristic of death-related disease resistance genes) and four NBS motifs. A tryptophan residue at the kinase-2 motif was indicative of the non-TIR-NBS class of proteins. Phylogenetic analysis revealed two major clusters. The seven Pigeon Pea RGAs were in a non-TIR group alongside wilt resistance proteins from tomato. Specific primers were designed against the RGAs identified by BLASTN, and these successfully amplified sequences from all eight Pigeon Pea genotypes. The 40 resultant sequences were combined according to genotype and subjected to phylogenetic analysis. Genotypes clustered according to breeding pedigree. Multiple alignments of the 40 sequences revealed several single nucleotide polymorphisms (SNPs) that are useful in identifying candidate resistance genes associated with FW and SMD.