scholarly journals KERAGAMAN GENETIK KELAPA DALAM MAPANGET NOMOR 32 HASIL PENYERBUKAN SENDIRI BERDASARKAN PENANDA RAPD

2020 ◽  
Vol 7 (2) ◽  
pp. 43
Author(s):  
HENGKY NOVARJANTO ◽  
J. KUMAUNANG ◽  
M. A. TULALO ◽  
A. MASNIAWATI ◽  
A. HARTANA

<p><strong>Genetic variability of selfing Mapanget Tall coconut No. 32 based on RAPD marker</strong></p><p>The objective of this study was to analyze the genetic variability of seling Mapanget Tall coconut No. 32 used RAPD marker. Ihe method of morphology, fruit component and isozymc analyses could not explain the homozygote level of the offspring and his parents. The DNA analysis was done at Plant Biology Laboratory, PAU, Life Science IPB, and the coconut leaflets samples were collected from Kima Atas Research Instalation, Research Institute for Coconut and Palmae, Manado. This research the study was conducted from November 1999 to Fcbruay 2000. Coconut materials analyzed were DMT 32-OP, DMT 32-S2, DM 1 32-S3 andDMT32-S4. DMT 32-S2 was the offsprings of the selfcd DMT 32- SI coconut seling. and the DMT 32-SI came from the sclfed of DMT 32-OP. Then selfcd DMT 32-S2 produced were found the DMT 32-S3. and selfcd of DMT 32-S3 produced the progeny of DMT 32-S4. DNA was isolated using the method of ROHDE et at (1995), while DNA quantity and quality was using the method of SAMBROOK et al (1989). Then the DNA was ampliied using 10 random primer 10 mer and PCR apparatus of 2.400 Perkin-Elmer System. Ater thai the DNA was elcctrophorated, and photographed using Polaroid 667 ilm, then ihe biner data matrix of each coconut population was calculated lor Ilic number of monomorphism banding was found in DMT 32-S2. Ihe genetic similarity between DMT 32-S3 and DMT 32-S3 was the mosl similar at genetic distance of 90%. DMT 32-S3 resulted from self pollination can be recommended as parent material for hybridization.</p>

2016 ◽  
Vol 97 (6) ◽  
pp. 1307-1315 ◽  
Author(s):  
Elangovan Dilipan ◽  
Jutta Papenbrock ◽  
Thirunavakkarasu Thangaradjou

In India 14 seagrass species can be found with monospecific genera (Enhalus, ThalassiaandSyringodium),Cymodoceawith two species andHalophilaandHalodulerepresented by more than two taxonomically complex species. Considering this, the present study was made to understand the level and pattern of genetic variability among these species collected from Tamilnadu coast, India. Random amplified polymorphic DNA (RAPD) analysis was used to evaluate the level of polymorphism existing between the species. Out of the 12 primers tested, 10 primers amplified 415 DNA fragments with an average of 41.5 fragments per primer. Of the total 415 amplified fragments only 123 (29.7%) were monomorphic and the remaining 292 (70.3%) were polymorphic for Indian seagrass species. Among the 10 primers used four are identified as the key primers capable of distinguishing all the Indian seagrasses with a high degree of polymorphism and bringing representative polymorphic alleles in all the tested seagrasses. From the present investigation, this study shows that the RAPD marker technique can be used not only as a tool to analyse genetic diversity but also to resolve the taxonomic uncertainties existing in the Indian seagrasses. The efficiency of these primers in bringing out the genetic polymorphism or homogeneity among different populations of theHalophilaandHalodulecomplex still has to be tested before recommending these primers as an identification tool for Indian seagrasses.


1988 ◽  
Vol 66 (3) ◽  
pp. 588-594 ◽  
Author(s):  
Hong Zhu ◽  
Kenneth O. Higginbotham ◽  
Bruce P. Dancik ◽  
Stan Navratil

Mycelial extracts of 43 isolates of Suillus tomentosus (Kauffm.) Singer, Snell & Dick collected from four boreal forest regions in Alberta were subjected to starch gel electrophoresis. A total of 21 bands was resolved from eight different enzyme systems presumably representing 13 loci. Six loci were polymorphic among these isolates. Cluster and principal components analyses demonstrated that intraspecific genetic variability of this fungus existed among and within forest regions. Polymorphic loci of acid phosphatase and alkaline phosphatase exhibited the greatest genetic similarity among the isolates within forest regions. Habitat isolation and host selection could be the major sources of genetic variation among forest regions.


Author(s):  
Thien Minh Nguyen ◽  
Tien Thi My Pham

The agronomic values of this population have been evaluated in the field experiments based on their phenotypic performance of agronomic traits, but the genetic variability of this population needs to be evaluated via techniques based on genetic material - DNA. In this study, the genetic variability in the investigated population of 71 hybrids and their parents was evaluated by RAPD technique, using eight selected arbitrarily primers; Genetic parameters and dendrogram expressing the genetic relationships among the investigated population were analyzed by GenALEx 6.1, Popgene 1.31 and NTSYSpc 2.1 softwares. Eight primers were used to generate the amplify products on each individual in the investigated population. From 74 genotypes, a total of 109 fragments were generated, among which, there were 89 polymorphic bands representing 81.65% with an average of 11 polymorphic bands/primer. Genetic similarity coefficient among the investigated population, based on DICE coefficient, ranged from 0.560 (LH05/0822 and PB260) to 0.991 (LH05/0781 and LH05/0841) with an average of 0,796, meaning that the genetic distance among ranged from 0.009 to 0.440 with an average of 0.231. The Shannon index and mean heterozygosity values were 0.328 and 0,176, respectively. This indicated that the progenies of the two investigated crosses possessed a relatively high range of genetic variability. The analysis of molecular variance (AMOVA) showed that genetic variation within population represented 62%, while genetic variation among two different crosses contributes 38% to the total genetic variability. Dendrogram based on DICE’s genetic similarity using UPGMA method showed that the hybrids divide into two major genetic groups (0.75), but the crosses were scattered independently of the hybrid.


2013 ◽  
Vol 43 (6) ◽  
pp. 978-984 ◽  
Author(s):  
Vanice Dias Oliveira ◽  
Allivia Rouse Carregosa Rabbani ◽  
Ana Veruska Cruz da Silva ◽  
Ana da Silva Lédo

This research had as objective to characterize genetically individuals of physic nut cultivated in experimental areas in Sergipe, Brazil by means of RAPD molecular markers. Leaves of 40 individuals were collected and DNA was isolated using CTAB 2% method. Were used 30 primers RAPD for DNA amplification, and this data was used to estimate the genetic similarity among the pairs of individuals, using Jaccard coefficient, and group them out for the UPGMA method. Also, the genetic structure and diversity of the populations were assessed using AMOVA. Of the 100 fragments generated, 29 of were polymorphic. A similarity average of 0.54 among the individuals was found and the amplitude similarities varied from 0.18 to 1.00. One of them (U5) was unit clusters and formed by the most divergent individuals. AMOVA indicated that there is more variation within (63%) the population. In conclusion, it was possible verify genetic variability in physic nut using RAPD markers at these experimental areas.


2020 ◽  
Vol 4 (2) ◽  
pp. 57-62
Author(s):  
IRFAN MARTIANSYAH ◽  
NURHAIMI HARIS ◽  
TATI HUSNIYATI ◽  
EDI DJAUHARI PURWAKUSUMAH

The rubber seeds are insufficient for producing rootstocks to rubber grafting. It can be overcome by an in vitro micro-cutting culture technique developed in the Indonesian Research Institute for Biotechnology and Bioindustry (IRIBB). However, the origin clone of 57 rubber genotypes used as an explant source in vitro micro-cutting culture is not recognized. The study was to investigate the 57 genotypes that came from mixed GT 1, PB 260, and RRIM 600 as parent clones. We investigated using seven primers of Random Amplified Polymorphic DNA (RAPD), i.e., OPA 02, OPA 07, OPA 15, OPB 04, OPC 05, OPC 11, and OPC 20. The qualitative analyzed by electrophoresis 1% gel agarose. A total of 47 DNA fragments produced with an average of 7 fragments per primer. OPA 02 generated of 13 fragments, whereas OPB 04 only one fragment. The DNA fragment pattern shows the presence of polymorphism. The genetic similarity coefficients obtained in the range of 62-96%. The highest genetic similarity (96%) is genotype 70 and 78. It recognized that 42 genotypes from 57 rubber genotypes had the closest relationship with PB 260 clones. Furthermore, six genotypes had a significant growth response as an explant in vitro micro-cutting culture.


2002 ◽  
Vol 62 (3) ◽  
pp. 503-508 ◽  
Author(s):  
N. MORAES ◽  
J. S. MORGANTE ◽  
C. Y. MIYAKI

In this study we analyzed a population of Bradypus torquatus with individuals originally distributed in different localities of Bahia, and two populations of B. variegatus with individuals from Bahia and São Paulo States. Using the DNA fingerprinting method, we assessed the genetic variability within and between populations. Analysis of the DNA profiles revealed genetic similarity indices ranging from 0.34 ± 0.07 to 0.87 ± 0.04. Similar low levels of genetic variability were found only in isolated mammalian populations or among related individuals. This study presents the first analyses of genetic diversity in sloth populations.


2019 ◽  
Vol 47 (3) ◽  
pp. 947-953
Author(s):  
Izabela SZUĆKO ◽  
Anna MĄDRACH

The increasing use of triticale (× Triticosecale Wittmack) indicates that its position on the seed market is constantly strengthening; therefore, the research on its genetic variability is necessary to improve breeding process of new cultivars. The aim of the study was to assess the possibility of using the ITAP-PCR technique to analyse the genetic similarity of nine cultivars of winter triticale cultivated in Poland. Primers designed on the basis of 6 DNA transposon sequences commonly found in cereal plant genomes were used for the study. The average polymorphism rate in the genotypes used in the study was determined as 95.24%; in total, 75 bands were obtained, of which 73 were polymorphic. The PIC value ranged between 0.27 and 0.44, and was highest for the Hamlet primer. The lowest PIC value was observed for the Mutator primer. The average DI value was 0.34, MI - 4.08, AEI - 12.17 and IPI - 4.40. SI ranged from 36.7% to 1.7%. A dendrogram was created according to the unweighted pair group method with arithmetic mean (UPGMA), which in terms of genetic similarity divided the analysed winter triticale cultivars into two main similarity groups.We confirmed that ITAP technique of transposon-based marker is efficient and fast method to detect genetic variability between different winter triticale cultivars. In addition, the presence of analyzed transposon families in hexaploid triticale has not been studied earlier.


2012 ◽  
Vol 9 (2) ◽  
pp. 217-220 ◽  
Author(s):  
KN Monira ◽  
MN Islam ◽  
R Khatun ◽  
S Ahmed

Random amplified polymorphism DNA (RAPD) technique was applied to detect genetic similarity between seven local  chicken strains selected for eggs and meat production in Bangladesh. Conservation and improvement strategies     ought to be based on proper genetic characterization in association with phenotypic characterization. White Leghorn, White Rock, Rhode Island Red, and Barred Plymouth Rock fall under recognized strain and Hilly, Deshi and Necked Neck fall under native bird group. Based on four oligonucleotide primers, the genetic similarity between the eggproducing strains (White Leghorn; White Rock; Rhode Island Red and Barred Plymouth Rock) was between 81.3 to 89.3 %. While the genetic similarity of three native chicken strains selected for meat production (Hilly, Deshi and Necked Neck) was 69.0 to 78.7 % similar based on the RAPD Marker. So, RAPD markers appeared to be effective in detecting similarity between chicken strains and they provide a potential tool for studying the inter-strain genetic similarity.   DOI: http://dx.doi.org/10.3329/jbau.v9i2.10989   J. Bangladesh Agril. Univ. 9(2): 217–220, 2011


Microbiology ◽  
2000 ◽  
Vol 81 (1) ◽  
pp. 171-179 ◽  
Author(s):  
Tony L. Goldberg ◽  
Edwin C. Hahn ◽  
Ronald M. Weigel ◽  
Gail Scherba

Porcine reproductive and respiratory syndrome virus (PRRSV) ORF5 gene sequences were generated by RT–PCR from 55 field isolates collected in Illinois and eastern Iowa. Spatial and temporal patterns of genetic variation in the virus were examined on a local geographical scale in order to test the hypothesis that the genetic similarity of PRRSV isolates (measured as their percentage pairwise ORF5 nucleotide similarity) was positively correlated with their geographical proximity. Levels of genetic variability in the Illinois/eastern Iowa PRRSV sample were similar to levels of variability seen across broader geographical regions within North America. The genetic similarity of isolates did not correlate with their geographical distance. These results imply that the movement of PRRSV onto farms does not generally occur via distance-limited processes such as wind or wildlife vectors, but more typically occurs via the long-distance transport of animals or semen. Genetic distances between PRRSV isolates collected from the same farms at different times increased as the time separating the collection events increased. This result implies rapid movement of new genetic types of PRRSV into and out of farms. PRRSV ORF5 displayed a pattern of third-codon-position diversity bias that was not evident in a geographically comparable sample of pseudorabies virus (a swine alphaherpesvirus) gC gene sequences. This result provides evidence that PRRSV ORF5 is experiencing stabilizing selection against structural novelty. Despite high genetic variability at all geographical levels, PRRSV ORF5 nevertheless contained potentially antigenic regions that were invariant at the amino acid level. These regions should make effective vaccine targets if they prove to be immunogenic.


Diversity ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 174 ◽  
Author(s):  
Khanshour ◽  
Hempsey ◽  
Juras ◽  
Cothran

The Cleveland Bay (CB) is the United Kingdom’s oldest established horse breed. In this study we analyzed the genetic variability in CB horses and investigated its genetic relationships with other horse breeds. We examined the genetic variability among 90 CB horses sampled in the USA compared to a total of 3447 horses from 59 other breeds. Analysis of the genetic diversity and population structure was carried out using 15 microsatellite loci. We found that genetic diversity in CB horses was less than that for the majority of other tested breeds. The genetic similarity measures showed no direct relationship between the CB and Thoroughbred but suggested the Turkman horses (likely in the lineage of ancestors of the Thoroughbred) as a possible ancestor. Our findings reveal the genetic uniqueness of the CB breed and indicate its need to be preserved as a genetic resource.


Sign in / Sign up

Export Citation Format

Share Document