A set of universal primers for amplification of polymorphic non-coding regions of mitochondrial and chloroplast DNA in plants

1995 ◽  
Vol 4 (1) ◽  
pp. 129-134 ◽  
Author(s):  
B. DEMESURE ◽  
N. SODZI ◽  
R. J. PETIT
1991 ◽  
Vol 17 (5) ◽  
pp. 1105-1109 ◽  
Author(s):  
Pierre Taberlet ◽  
Ludovic Gielly ◽  
Guy Pautou ◽  
Jean Bouvet

2015 ◽  
Vol 10 (1) ◽  
Author(s):  
L. Skuza ◽  
E. Filip ◽  
I. Szućko

AbstractNon-coding rDNA spacers (IGS) can vary substantially in size due to differences in the number of repetitive elements among closely related species. Three pairs of universal primers were used in this study for the amplification of non-coding regions of ribosomal (rRNA) IGS. The amplified IGS products obtained from 19 Secale accessions, which included both cultivated and noncultivated rye and which represented three species and four subspecies of the genus Secale, showed a high level of polymorphism. The PCR results were characterized by multiple bands (1-6), different sizes (750bp-3250bp) and 100% polymorphism. Cluster analysis using the neighborjoining method based on the Dice’s coefficient of genetic similarity showed a division of the studied species into two similarity groups. All the studied Secale cereale ssp. cereale were found to belong to the same similarity group. The variation in the size of the IGS among the species which was detected in this study could be due to dissimilarity between the sequences of their respective repetitive elements or between their tandem repeat numbers. The highly interspecific polymorphisms for the rDNA IGS regions suggested that IGS might be a useful molecular marker in studies of Secale species.


2010 ◽  
Vol 125 (3) ◽  
pp. 512-517 ◽  
Author(s):  
Ghada Baraket ◽  
Ahmed Ben Abdelkrim ◽  
Olfa Saddoud ◽  
Khaled Chatti ◽  
Messaoud Mars ◽  
...  

Genome ◽  
2000 ◽  
Vol 43 (4) ◽  
pp. 634-641 ◽  
Author(s):  
T HM Mes ◽  
P Kuperus ◽  
J Kirschner ◽  
J Stepanek ◽  
P Oosterveld ◽  
...  

Sequence variation in 2.2 kb of non-coding regions of the chloroplast genome of eight dandelions (Taraxacum: Lactuceae) from Asia and Europe is interpreted in the light of the phylogenetic signal of base substitutions vs. indels (insertions-deletions). The four non-coding regions displayed a total of approximately 30 structural mutations of which 9 are potentially phylogenetically informative. Insertions, deletions, and an inversion were found that involved consecutive stretches of up to 172 bases. When compared to phylogenetic relationships of the chloroplast genomes based on nucleotide substitutions only, many homoplasious indels (33%) were detected that differed considerably in length and did not comprise simple sequence repeats typically associated with replication slippage. Though many indels in the intergenic spacers were associated with direct repeats, frequently, the variable stretches participated in inverted repeat stabilized hairpins. In each intergenic spacer or intron examined, nucleotide stretches ranging from 30 to 60 bp were able to fold into stabilized secondary structures. When these indels were homoplasious, they always ranked among the most stabilized hairpins in the non-coding regions. The association of higher order structures that involve both classes of repeats and parallel structural mutations in hot spot regions of the chloroplast genome can be used to differentiate among mutations that differ in phylogenetic reliability.Key words: Taraxacum, indel, non-coding chloroplast DNA, hairpin, evolution.


2016 ◽  
Vol 14 (1) ◽  
pp. 31-37 ◽  
Author(s):  
Majid Talebi ◽  
Mohammad Akbari ◽  
Maryam Zamani ◽  
Badraldin Ebrahim Sayed-Tabatabaei

1996 ◽  
Vol 30 (3) ◽  
pp. 259-262 ◽  
Author(s):  
Scot A. Kelchner ◽  
J. F. Wendel

2018 ◽  
Vol 47 (1) ◽  
pp. 54-62 ◽  
Author(s):  
Lidia SKUZA ◽  
Izabela SZUĆKO ◽  
Ewa FILIP ◽  
Anastazja ADAMCZYK

DNA barcoding is a relatively new method of identifying plant species using short sequences of chloroplast DNA. Although there is a large number of studies using barcoding on various plant species, there are no such studies in the genus Secale. In this study the plant material consisted of 10 cultivated and non-cultivated species and subspecies of rye genus. Three chloroplast DNA regions (rbcL, matK, trnH-psbA) were tested for their suitability as DNA barcoding regions. Universal primers were used, and sequenced products were analyzed using Neighbor Joining and the Maximum Likelihood in the MEGA 7.1 program. We did not observe high variability in nucleotide sequences within the matK and rbcL regions. Only 2.2% of the sequences showed polymorphism in the rbcL region, while 6.5% in the matK region. The most variable trnH-psbA (15.6%) intergenic region was the most useful for rye barcoding. Individual application of the studied regions did not provide the expected results. None of the regions used in the study allowed the division of rye species and subspecies according to the adopted classification of the genus Secale. The results confirm that the use of matK and rbcL is insufficient for DNA barcoding in rye species, and better discrimination within the genus Secale can be obtained only in combination with the non-coding trnH-psbA sequence. Our results also indicate the necessity of using a different region. All of the new sequences have been deposited in Genbank.


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