Chloroplast DNA codes for tRNA from cytoplasmic polyribosomes

Nature ◽  
1978 ◽  
Vol 274 (5672) ◽  
pp. 717-719 ◽  
Author(s):  
JAN MILLER McCREA ◽  
CHARLES L. HERSHBERGER
Keyword(s):  
Chloroplast Dna ◽  
Dna Codes

scholarly journals Chloroplast DNA codes for transfer RNA

1976 ◽  
Vol 3 (8) ◽  
pp. 2005-2018 ◽  
Author(s):  
J. M. McCrea ◽  
C. L. Hershberger
Keyword(s):  
Chloroplast Dna ◽  
Transfer Rna ◽  
Dna Codes

scholarly journals Euglena gracilis Chloroplast DNA Codes for Polyadenylated RNA

1979 ◽  
Vol 64 (5) ◽  
pp. 818-821 ◽  
Author(s):  
Joel J. Milner ◽  
Charles L. Hershberger ◽  
Dennis E. Buetow
Keyword(s):  
Chloroplast Dna ◽  
Euglena Gracilis ◽  
Dna Codes ◽  
Polyadenylated Rna

Phylogenetic position ofKontumia(Polypodiaceae) inferred from four chloroplast DNA regions

2012 ◽  
pp. n/a-n/a
Author(s):  
Changkyun Kim ◽  
Hong-Guang Zha ◽  
Tao Deng ◽  
Hang Sun ◽  
Su-Gong Wu
Keyword(s):  
Chloroplast Dna ◽  
Phylogenetic Position ◽  
Chloroplast Dna Regions

Spatial Patterns of Chloroplast DNA and Cone Morphology Variation within Populations of a Pinus banksiana-Pinus contorta Sympatric Region

1991 ◽  
Vol 138 (1) ◽  
pp. 156-170 ◽  
Author(s):  
David B. Wagner ◽  
Zhong-Xu Sun ◽  
Diddahally R. Govindaraju ◽  
Bruce P. Dancik
Keyword(s):  
Chloroplast Dna ◽  
Spatial Patterns ◽  
Pinus Banksiana ◽  
Pinus Contorta ◽  
Cone Morphology

scholarly journals Molecular variation in chloroplast DNA regions in ancestral species of wheat.

Genetics ◽  
1994 ◽  
Vol 137 (3) ◽  
pp. 883-889 ◽  
Author(s):  
N T Miyashita ◽  
N Mori ◽  
K Tsunewaki
Keyword(s):  
Chloroplast Dna ◽  
Restriction Enzymes ◽  
Triticum Dicoccoides ◽  
The Other ◽  
Major Type ◽  
Aegilops Speltoides ◽  
Triticum Timopheevi ◽  
Restriction Sites ◽  
D Values ◽  
Chloroplast Dna Regions

Abstract Restriction map variation in two 5-6-kb chloroplast DNA regions of five diploid Aegilops species in the section Sitopsis and two wild tetraploid wheats, Triticum dicoccoides and Triticum araraticum, was investigated with a battery of four-cutter restriction enzymes. A single accession each of Triticum durum, Triticum timopheevi and Triticum aestivum was included as a reference. More than 250 restriction sites were scored, of which only seven sites were found polymorphic in Aegilops speltoides. No restriction site polymorphisms were detected in all of the other diploid and tetraploid species. In addition, six insertion/deletion polymorphisms were detected, but they were mostly unique or species-specific. Estimated nucleotide diversity was 0.0006 for A. speltoides, and 0.0000 for all the other investigated species. In A. speltoides, none of Tajima's D values was significant, indicating no clear deviation from the neutrality of molecular polymorphisms. Significant non-random association was detected for three combinations out of 10 possible pairs between polymorphic restriction sites in A. speltoides. Phylogenetic relationship among all the plastotypes (plastid genotype) suggested the diphyletic origin of T. dicoccoides and T. araraticum. A plastotype of one A. speltoides accession was identical to the major type of T. araraticum (T. timopheevi inclusively). Three of the plastotypes found in the Sitopsis species are very similar, but not identical, to that of T. dicoccoides, T. durum and T. aestivum.

scholarly journals Phylogeography of Prunus armeniaca L. revealed by chloroplast DNA and nuclear ribosomal sequences

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Wen-Wen Li ◽  
Li-Qiang Liu ◽  
Qiu-Ping Zhang ◽  
Wei-Quan Zhou ◽  
Guo-Quan Fan ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Genetic Variation ◽  
Chloroplast Dna ◽  
Population Expansion ◽  
Prunus Armeniaca ◽  
River Valley ◽  
Nuclear Ribosomal Dna ◽  
Glacial Refugium ◽  
Ili River Valley ◽  
Wild Apricot

AbstractTo clarify the phytogeography of Prunus armeniaca L., two chloroplast DNA fragments (trnL-trnF and ycf1) and the nuclear ribosomal DNA internal transcribed spacer (ITS) were employed to assess genetic variation across 12 P. armeniaca populations. The results of cpDNA and ITS sequence data analysis showed a high the level of genetic diversity (cpDNA: HT = 0.499; ITS: HT = 0.876) and a low level of genetic differentiation (cpDNA: FST = 0.1628; ITS: FST = 0.0297) in P. armeniaca. Analysis of molecular variance (AMOVA) revealed that most of the genetic variation in P. armeniaca occurred among individuals within populations. The value of interpopulation differentiation (NST) was significantly higher than the number of substitution types (GST), indicating genealogical structure in P. armeniaca. P. armeniaca shared genotypes with related species and may be associated with them through continuous and extensive gene flow. The haplotypes/genotypes of cultivated apricot populations in Xinjiang, North China, and foreign apricot populations were mixed with large numbers of haplotypes/genotypes of wild apricot populations from the Ili River Valley. The wild apricot populations in the Ili River Valley contained the ancestral haplotypes/genotypes with the highest genetic diversity and were located in an area considered a potential glacial refugium for P. armeniaca. Since population expansion occurred 16.53 kyr ago, the area has provided a suitable climate for the population and protected the genetic diversity of P. armeniaca.

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