Molecular diversity analysis and DNA fingerprinting of cotton varieties of India

2020 ◽  
Vol 79 (04) ◽  
Author(s):  
V. Santhy ◽  
M. Meshram ◽  
H. B. Santosh ◽  
K. R. Kranthi
Keyword(s):  
Dna Fingerprinting ◽  
Ssr Markers ◽  
Goodness Of Fit ◽  
Molecular Diversity ◽  
Cultivar Identification ◽  
Similarity Index ◽  
Dna Fingerprint ◽  
Tetraploid Cotton ◽  
Linkage Groups ◽  
Jaccard's Similarity Index

Genetic diversity was assessed in 48 popular varieties of tetraploid cotton from each cultivated zone of India using 68 SSR markers distributed across linkage groups. The markers produced a total of 144 alleles with an average of 2.19 per locus. The polymorphism information content (PIC) ranged from 0.04 to 0.57 with a mean of 0.23 indicating lesser diversity in the studied material. Jaccard’s similarity index based neighbourhood joining cluster analysis grouped the genotypes into three major clusters, each of which was further classified into sub-groups. Inconsistencies were observed between the clusters and known pedigree of the cultivars. A narrow genetic base was also revealed among the cotton cultivars. The SSR markers revealed a genetic similarity of 73% among the varieties studied. The DNA fingerprint developed using a selected set of 14 markers showed a probability of identical match of 2.47×10-3 with high goodness of fit (r2=0.86). The identified markers have great potential in DNA fingerprinting in cotton which in future could be integrated with DUS data descriptors for effective cultivar identification and differentiation.

scholarly journals Characterization of Little millet (Panicum sumatrense) varieties using Morphological descriptors and SSR based DNA fingerprinting

2020 ◽  
pp. 29-34
Author(s):  
Senthil Natesan ◽  
Gayathri Venugopalan ◽  
Selva Babu Selvamani ◽  
Madhumitha Krishnamoorthy ◽  
Sarankumar Chandran ◽  
...  
Keyword(s):  
Dna Fingerprinting ◽  
Pearl Millet ◽  
Ssr Markers ◽  
Morphological Characters ◽  
Dna Fingerprint ◽  
Morphological Descriptors ◽  
Little Millet ◽  
Amplicon Size ◽  
Cereal Genomes ◽  
Unique Markers

Little millet varieties are generally distinguished by morphological descriptors which are being used for seed certification and DUS characterization [1]. But in practical terms, these key differentiation descriptors between varieties of little millet are very fewer and hence difficult to differentiate germplasm accessions. Germplasm registration in NBPGR needs DNA fingerprint to show the uniqueness of germplasm in comparison to existing varieties. DNA fingerprinting is a better option to identify unique markers to differentiate the varieties. Available genomic resources are scarce since little millet is still considered to be an orphan crop. Therefore markers from other cereal genomes such as maize, pearl millet and barnyard millet that are been utilized for DNA fingerprinting purpose with a clue of cereal synteny relationship. Twenty-one morphological descriptors studies revealed that the variety ATL 1 is different from the other varieties for more than 16 morphological characters studied. DNA fingerprinting is attempted in five genotypes of little millets such as BL6, ATL 1, TNPsu 176, Co (Samai) 4, Paiyur 2 using cereal SSR markers. Among the 25 maize SSR markers used two markers viz., phi213984 and phi295450 scored polymorphism by the amplicon size of 310bp and 600bp respectively. From the 25 Pearl millet SSR markers used only one SSR marker found polymorphic at 305bp allele size for ATL 1 and Hence, SSR based DNA fingerprinting helped to differentiate ATL1, the newly released high yielding variety from other genotypes of little millets which can be used for varietal identification purpose.

scholarly journals Microsatellite Marker Development in Rose and its Application in Tetraploid Mapping

2006 ◽  
Vol 131 (3) ◽  
pp. 380-387 ◽  
Author(s):  
L.H. Zhang ◽  
D.H. Byrne ◽  
R.E. Ballard ◽  
S. Rajapakse
Keyword(s):  
Ssr Markers ◽  
Genomic Library ◽  
Cultivar Identification ◽  
Genetic Maps ◽  
Linkage Groups ◽  
Specific Primers ◽  
Pcr Products ◽  
Ssr Loci ◽  
Tetraploid Parent ◽  
Simple Sequence

Microsatellite or simple sequence repeat (SSR) markers were developed from Rosa wichurana Crépin to combine two previously constructed tetraploid rose (Rosa hybrida L.) genetic maps. To isolate SSR-containing sequences from rose a small-insert genomic library was constructed from diploid Rosa wichurana and screened with several SSR probes. Specific primers were designed for 43 unique SSR regions, of which 30 primer pairs gave rise to clear PCR products. Seventeen SSR primer pairs (57%) produced polymorphism in the tetraploid rose 90-69 mapping family. These markers were incorporated into existing maps of the parents 86-7 and 82-1134, which were constructed primarily with AFLP markers. The current map of the male parent, amphidiploid 86-7, consists of 286 markers assigned to 14 linkage groups and covering 770 cm. The map of the female tetraploid parent, 82-1134, consists of 256 markers assigned to 20 linkage groups and covering 920 cm. Nineteen rose SSR loci were mapped on the 86-7 map and 11 on the 82-1134 map. Several homeologous linkage groups within maps were identified based on SSR markers. In addition, some of the SSR markers provided anchoring points between the two parental maps. SSR markers were also useful for joining small linkage groups. Based on shared SSR markers, consensus orders for four rose linkage groups between parental maps were generated. Microsatellite markers developed in this study will provide valuable tools for many aspects of rose research including future consolidation of diploid and tetraploid rose genetic linkage maps, genetic, phylogenetic and population analyses, cultivar identification, and marker-assisted selection.

Identification of chickpea cultivars by microsatellite markers

2010 ◽  
Vol 149 (4) ◽  
pp. 451-460 ◽  
Author(s):  
P. CASTRO ◽  
T. MILLÁN ◽  
J. GIL ◽  
J. MÉRIDA ◽  
M. L. GARCÍA ◽  
...  
Keyword(s):  
Microsatellite Markers ◽  
Cultivar Identification ◽  
Polymorphic Information Content ◽  
Morphological Characteristics ◽  
Dna Fingerprint ◽  
Linkage Groups ◽  
Chickpea Cultivar ◽  
High Level ◽  
Chickpea Cultivars

SUMMARYCharacterization of plant varieties is traditionally based on phenotypic observation. However, some varieties have very similar morphological characteristics, which make it difficult to distinguish between them. The present study employed 15 microsatellite markers distributed across all linkage groups (LG) of the chickpea genetic map to characterize 32 commercial chickpea cultivars and determine the usefulness of these markers for cultivar identification. These markers showed a high level of polymorphism; a total of 154 different alleles were detected, with a mean of 10·3 alleles per locus. The polymorphic information content (PIC) value ranged from 0·455 to 0·897. All the markers, with the exception of TA130, TA135 and TA144, were considered to be informative (PIC>0·7), indicating their potential usefulness for cultivar identification. A subset of markers (TA186, TA200, TA106, TA113, TA117 and TA30) was sufficient to identify all the cultivars studied. In order to confirm their discriminatory power, 16 unreleased chickpea cultivars (V1–V16) were screened and all of them presented different patterns. Therefore, these microsatellites can be regarded as a reference set for chickpea cultivar identification and their profiles can be used as a DNA fingerprint for each registered cultivar, avoiding redundancy of identical cultivars as well as to protect breeders' rights.

LEGITIMACY OF PROGENIES USING SSR MARKERS AS CONTROLLING SYSTEM AND EARLIER SELECTION IN THE OIL PALM NURSERY (Elaeis guineensis JACQ.)

2018 ◽  
Vol 25 (1) ◽  
pp. 21-30
Author(s):  
Rokhana Faizah ◽  
Sri Wening ◽  
Abdul Razak Purba
Keyword(s):  
Dna Fingerprinting ◽  
Ssr Markers ◽  
Oil Palm ◽  
Dna Markers ◽  
Elaeis Guineensis ◽  
Gene Marker ◽  
Controlling System ◽  
Crossing Probability ◽  
Simple Sequence

Information of legitimacy of oil palm progenies is important to guaranty the quality and to control commercial seeds procedures. A true and legitimate cross will produce progeny which has a combination of their parent's allele. The information could be obtained early in the nursery stage through DNA fingerprinting analysis. Simple Sequence Repeats (SSR) is one of DNA markers used for DNA fingerprinting, since the marker system has advantages to acquire information of allele per individual in population and efficiency diverse allele of progeny and their parents. The aim of the research is to obtain legitimacy of 12 progenies analyzing in the oil palm nursery stage. Thirteen SSR markers were used to analyze 12 crossings number of oil palm. The genotypes data by alleles of SSR inferred and quantified using Gene Marker® Software version 2.4.0 Soft Genetics® LLC and analyzed based on Mendel's Law of Segregation. The result showed based on heredity pattern of progeny and their parent's allele that progenies H were indicated genetically derived from their known parents while progenies from A and G indicated as illegitimate crossing. Probability value for legitimacy of progenies of 9 other crosses has 0.031 and 0.5. Legitimacy analysis of progeny using SSR markers could be used to control the quality of crossing material and earlier selection in the oil palm nursery.

scholarly journals Genetic Diversity of Selected Rice Genotypes under Water Stress Conditions

Plants ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 27
Author(s):  
Mahmoud M. Gaballah ◽  
Azza M. Metwally ◽  
Milan Skalicky ◽  
Mohamed M. Hassan ◽  
Marian Brestic ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Water Stress ◽  
Drought Stress ◽  
Drought Tolerance ◽  
Ssr Markers ◽  
Similarity Index ◽  
Stress Conditions ◽  
Yield Potential ◽  
Drought Tolerant ◽  
Rice Genotypes

Drought is the most challenging abiotic stress for rice production in the world. Thus, developing new rice genotype tolerance to water scarcity is one of the best strategies to achieve and maximize high yield potential with water savings. The study aims to characterize 16 rice genotypes for grain and agronomic parameters under normal and drought stress conditions, and genetic differentiation, by determining specific DNA markers related to drought tolerance using Simple Sequence Repeats (SSR) markers and grouping cultivars, establishing their genetic relationship for different traits. The experiment was conducted under irrigated (normal) and water stress conditions. Mean squares due to genotype × environment interactions were highly significant for major traits. For the number of panicles/plants, the genotypes Giza179, IET1444, Hybrid1, and Hybrid2 showed the maximum mean values. The required sterility percentage values were produced by genotypes IET1444, Giza178, Hybrid2, and Giza179, while, Sakha101, Giza179, Hybrid1, and Hybrid2 achieved the highest values of grain yield/plant. The genotypes Giza178, Giza179, Hybrid1, and Hybrid2, produced maximum values for water use efficiency. The effective number of alleles per locus ranged from 1.20 alleles to 3.0 alleles with an average of 1.28 alleles, and the He values for all SSR markers used varied from 0.94 to 1.00 with an average of 0.98. The polymorphic information content (PIC) values for the SSR were varied from 0.83 to 0.99, with an average of 0.95 along with a highly significant correlation between PIC values and the number of amplified alleles detected per locus. The highest similarity coefficient between Giza181 and Giza182 (Indica type) was observed and are susceptible to drought stress. High similarity percentage between the genotypes (japonica type; Sakha104 with Sakha102 and Sakha106 (0.45), Sakha101 with Sakha102 and Sakha106 (0.40), Sakha105 with Hybrid1 (0.40), Hybrid1 with Giza178 (0.40) and GZ1368-S-5-4 with Giza181 (0.40)) was also observed, which are also susceptible to drought stress. All genotypes are grouped into two major clusters in the dendrogram at 66% similarity based on Jaccard’s similarity index. The first cluster (A) was divided into two minor groups A1 and A2, in which A1 had two groups A1-1 and A1-2, containing drought-tolerant genotypes like IET1444, GZ1386-S-5-4 and Hybrid1. On the other hand, the A1-2 cluster divided into A1-2-1 containing Hybrid2 genotype and A1-2-2 containing Giza179 and Giza178 at coefficient 0.91, showing moderate tolerance to drought stress. The genotypes GZ1368-S-5-4, IET1444, Giza 178, and Giza179, could be included as appropriate materials for developing a drought-tolerant variety breeding program. Genetic diversity to grow new rice cultivars that combine drought tolerance with high grain yields is essential to maintaining food security.

scholarly journals Evidence of genetic heterogeneity in a BALB/c mouse colony as determined by DNA fingerprinting

1998 ◽  
Vol 32 (1) ◽  
pp. 80-85 ◽  
Author(s):  
F. Benavides ◽  
D. Cazalla ◽  
C. Pereira ◽  
A. Fontanals ◽  
M. Salaverri ◽  
...  
Keyword(s):  
Dna Fingerprinting ◽  
Genetic Heterogeneity ◽  
Flow Cytometric Analysis ◽  
Skin Grafting ◽  
Electrophoretic Analysis ◽  
Coat Colour ◽  
Dna Fingerprint ◽  
Line System ◽  
Flow Cytometric ◽  
Immunological Research

A genetic monitoring of the BALB/c mouse foundation colony in our animal facility was carried out. The techniques of choice were skin grafting, coat colour test, flow cytometric analysis for H2 antigens (loci H2-D and H2-A), electrophoretic analysis of isoenzymes (loci Idh1, Pep3, Es3 and Mod1), PCR-amplified microsatellites (loci Igh-V, Ngfg, Plau, Crp, Igh, D16Mit5, D3Mit49 and D17Mit16) and DNA fingerprinting (multilocus probes 33.6, 33.15 and (CAC)5). No evidence of genetic contamination was found, ruling out the possibility of an outcross with AKR, the other albino strain maintained at the facility. Nevertheless, DNA fingerprint patterns revealed evidence of genetic heterogeneity in four out of nine lines of the nucleus colony, interpreted as minisatellite mutations favoured for a single line system with more than 40 generations of separation from the ancestral pair. These mice are mainly used in cancer and immunological research within the institute.

scholarly journals Keragaman Genetik 96 Aksesi Plasma Nutfah Padi Berdasarkan 30 Marka SSR Terpaut Gen Pengatur Waktu Pembungaan (HD Genes)

2016 ◽  
Vol 7 (2) ◽  
pp. 76
Author(s):  
Dwinita Wikan Utami ◽  
Sutoro Sutoro ◽  
Nurul Hidayatun ◽  
Andari Risliawati ◽  
Ida Hanarida
Keyword(s):  
Genetic Diversity ◽  
Microsatellite Markers ◽  
Ssr Markers ◽  
Heading Date ◽  
Germplasm Collection ◽  
Dna Fingerprint ◽  
Early Maturity ◽  
Plant Variety ◽  
Variety Protection ◽  
Genetic Analyzer

<p>Genetic Diversity of 96 Accession of Rice Germplasm<br />Using 30 SSR Markers Linked to Heading Date Genes (HD<br />Genes). Dwinita W. Utami, Sutoro, Nurul Hidayatun,<br />Andari Risliawati, and Ida Hanarida. Rice with early<br />maturity is one of an important genetic resources in rice<br />germplasm collection. Characterization and identification of<br />genetic diversity is an important issue for plant variety protection.<br />Molecular identification by microsatellite markers<br />using Genetic Analyzer enables resolve of this issue. The<br />objective of this research is to identify the genetic diversity of<br />96 rice accessions based on their specific DNA fingerprint<br />using microsatellite markers. A total of 96 accessions consisting<br />of a diverse variety of maturity classification were<br />genotyped with 30 SSR markers linked to HD genes which<br />spread out in 12 chromosomes of rice geneome. The total<br />297 alleles were detected indicated the level of marker<br />informativeness. RM5607 generated 7 allele with the size<br />range from 103 to 197 and the highest PIC at 0.90. RM3571<br />(linked to HD12 gene) has a significant value associated with<br />varieties which have early maturity trait. Clustering analysis<br />showed the cluster based on Sub Species genome background<br />and on early maturity trait.</p>

scholarly journals Application of Microsatellite and Inter Simple Sequence Markers for Certifying Trueness to Type of Grafted Ramets and Clustering of Persian Walnut Varieties

2021 ◽  
Author(s):  
Masoomeh Hosseini Nickravesh ◽  
Kourosh Vahdati ◽  
fatemeh amini ◽  
Reza Amiri ◽  
Keith Woeste
Keyword(s):  
Ssr Markers ◽  
Issr Markers ◽  
Principal Coordinate Analysis ◽  
Dna Fingerprint ◽  
Polymorphic Ssrs ◽  
Persian Walnut ◽  
Inter Simple Sequence Repeats ◽  
Ssr Loci ◽  
Ssrs Markers ◽  
Simple Sequence

Abstract The utility of seventeen Microsatellite (SSR) markers and fifteen inter simple sequence repeats (ISSR) markers for the identification of twenty eight ramets of 11 varieties of walnut (Juglans regia) was explored. Thirty nine individual genomes were screened using 61 and 38 scorable fragments from SSR and ISSR markers, respectively. The least polymorphic SSR locus was WGA004 (two alleles) and the most polymorphic (5 alleles) was WGA276. Polymorphism information content values ranged from 0.08 (WGA004) to 0.43 (WGA032) in SSR markers and from 0.11 (AGA (AC)7) to 0.49 (CAC(TGT)5) in ISSR markers, with an average of 0.29 and 0.19, respectively. In most cases, grafted varieties with identical names also had the same microsatellites profile. The principal coordinate analysis and clustering (UPGMA) based on the combined marker set emphasized two failures in grafting or off-types, ramets identified as Serr 4 (S4) and Vina 1 (V1). The presence of two off-type ramets in the walnut research orchard emphasizes the importance of using molecular certification for proving true-to-type of walnut orchards. Using 13 polymorphic SSRs, we tabulated a DNA fingerprint chart of 11 walnut varieties. Except for ‘Chandler’, each cultivar could be distinguished using a combination of only two SSR loci. The 13 SSRs markers evaluated in this study could be used in future to identify clones produced from the varieties.

scholarly journals A Study of Zooplankton Community in Dukan Lake, Kurdistan Region-Iraq, with a New Record of Craspedacusta sowerbii Lankester (1880) Medusa (Cnidaria: Hydrozoa)

2017 ◽  
Vol 14 (4) ◽  
pp. 735-741 ◽  
Author(s):  
Baghdad Science Journal
Keyword(s):  
Similarity Index ◽  
Chemical Properties ◽  
Zooplankton Community ◽  
Ion Concentration ◽  
Hydrogen Ion Concentration ◽  
Alkaline Side ◽  
Physical And Chemical ◽  
First Time ◽  
Jaccard's Similarity Index ◽  
And Chemical Properties

A study of Zooplankton community has been carried out at four selected sites on Dukan Lake. Samples of water and zooplankton were collected monthly for the period from July 2015 to February 2016. Some physical and chemical properties of water were studied and the results showed that the air temperature were ranged from 0 to 36.16 °C, water temperature ranged from 2.83 to 34.66 °C, hydrogen ion concentration of studied sites were found to lie in alkaline side, it was ranged between 6.87 to 8.57, electrical conductivity ranged from 190.79 to 850.08 µs.cm­¹, turbidity ranged from 0.9-7.7 NTU, and dissolved oxygen from 3.3 to 6.8 mg.l-¹ while BOD5 were ranged from 0.53 to 34.66 mg.l-¹. Concerning to the zooplankton, 37 species were identified which belonged to Cladocera (48.38%), Copepod (43.28%), Rotifera (8.23%), Targigrada (0.08%) and Cnidaria (0.1%). The medusa of Craspedacusta sowerbii Lankester (1880) was recorded for the first time in Iraq. Regarding to zooplankton community, rotifer were ranged between 0 to 690.91 ind.m-3, Copepoda from 54.55 to 5927.27 ind.m-3 and Cladocera ranged from 18.18 to 6072.73 ind.m-3. According to Shanon-Weiner index, species diversity for zooplankton invertebrates was ranged from 0.325 to 1.091 bits/ind. Jaccard’s similarity index showed that the highest similarity was recorded between site (1) and site (4) with 40.74%.

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