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  • 1
    In: Genome, Canadian Science Publishing, Vol. 58, No. 2 ( 2015-02), p. 63-70
    Abstract: Intermediate wheatgrass (Thinopyrum intermedium (Host) Barkworth & D.R. Dewey), a segmental autoallohexaploid (2n = 6x = 42), is not only an important forage crop but also a valuable gene reservoir for wheat (Triticum aestivum L.) improvement. Throughout the scientific literature, there continues to be disagreement as to the origin of the different genomes in intermediate wheatgrass. Genotypic data obtained from newly developed EST-SSR primers derived from the putative progenitor diploid species Pseudoroegneria spicata (Pursh) Á. Löve (St genome), Thinopyrum bessarabicum (Savul. & Rayss) Á. Löve (J = J b = E b ), and Thinopyrum elongatum (Host) D. Dewey (E = J e = E e ) indicate that the V genome of Dasypyrum (Coss. & Durieu) T. Durand is not one of the three genomes in intermediate wheatgrass. Based on all available information in the literature and findings in this study, the genomic designation of intermediate wheatgrass should be changed to J vs J r St, where J vs and J r represent ancestral genomes of present-day J b of Th. bessarabicum and J e of Th. elongatum, with J vs being more ancient. Furthermore, the information suggests that the St genome in intermediate wheatgrass is most similar to the present-day St found in diploid species of Pseudoroegneria from Eurasia.
    Type of Medium: Online Resource
    ISSN: 0831-2796 , 1480-3321
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 2015
    detail.hit.zdb_id: 2020635-5
    SSG: 12
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  • 2
    In: International Journal of Plant Sciences, University of Chicago Press, Vol. 164, No. 1 ( 2003-01), p. 25-33
    Type of Medium: Online Resource
    ISSN: 1058-5893 , 1537-5315
    RVK:
    Language: English
    Publisher: University of Chicago Press
    Publication Date: 2003
    detail.hit.zdb_id: 2038675-8
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    Wiley ; 1986
    In:  Crop Science Vol. 26, No. 4 ( 1986-07), p. 723-727
    In: Crop Science, Wiley, Vol. 26, No. 4 ( 1986-07), p. 723-727
    Abstract: The alloploid nature of some tetraploid accessions of Pseudoroegneria tauri (Boiss. & Bal.) A. Löve and P. spicata (Pursh) A. Löve was investigated by conducting meiotic analyses of the following hybrids: P. tauri (2 n =28) ✕ P. libanotica (Hackel) D.R. Dewey (2 n =14, genomes SS); P. tauri ✕ P. spicata (2 n =14, genomes SS); P. tauri ✕ P. spicata (allo‐4 x , 2 n =28, genomes SSXX); P. tauri ✕ Agropyron cristatum (L.) Gaertn. (2 n =14, genomes PP); and P. tauri ✕ A. cristatum (2 n =28, genomes PPPP). Meiotic data of these hybrids showed that P. tauri possessed both the S and P genomes, and it had only the S genome in common with the allotetraploid P. spicata . Mitotic cells showed 14 short and 14 long chromosomes in P. tauri ; 14 short and 7 long chromosomes in P. tauri ✕ P. libanotica ; and 14 long and 7 short chromosomes in P. tauri ✕ A. cristatum . It is concluded that two tetraploid accessions of P. tauri from Iran used in this study have the PPSS genome formula in which the long chromosomes are those of the P genome and the short ones are those of the S genome. An unknown (X) genome present in allotetraploid P. spicata differs from both the S and the P genomes, and possibly is an H genome. This study revealed that the alloploid nature of P. tauri , and possibly some tetraploid P. spicata accessions, is not due to the presence of a Ph‐like genetic system because of the high frequencies of nonhomologous pairing or incomplete preferentiality observed in these triploid and tetraploid hybrids. In view of these findings, forage grass breeders should not use these amphiploids in crosses with autotetraploid species in the genus Pseudoroegneria . Taxonomists must find a way to classify the natural amphiploid species with PPSS genomes.
    Type of Medium: Online Resource
    ISSN: 0011-183X , 1435-0653
    Language: English
    Publisher: Wiley
    Publication Date: 1986
    detail.hit.zdb_id: 1480918-7
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  • 4
    Online Resource
    Online Resource
    Frontiers Media SA ; 2021
    In:  Frontiers in Plant Science Vol. 12 ( 2021-10-4)
    In: Frontiers in Plant Science, Frontiers Media SA, Vol. 12 ( 2021-10-4)
    Abstract: Plant artificial minichromosomes are the next-generation technology for plant genetic engineering and represent an independent platform for expressing foreign genes and the tools for studying the structure and function of chromosomes. Minichromosomes have been successfully produced by telomere-mediated chromosome truncation in several plants. However, previous studies have primarily focused on the construction and rough characterization of minichromosomes, while the development of stably inherited minichromosomes and their precise characterization and tracking over different generations have rarely been demonstrated. In this study, a 0.35-kb direct repeat of the Arabidopsis telomeric sequence was transformed into Brassica napus to produce artificial minichromosomes, which were analyzed by multifluorescence in situ hybridization (multi-FISH), Southern hybridization, and primer extension telomere rapid amplification (PETRA). The stably inherited minichromosomes C2 and C4 were developed by crossing transgenic plants with wild-type plants and then selfing the hybrids. Notably, two truncation sites on chromosomes C2 and C4, respectively, were identified by resequencing; thus, the artificial minichromosomes were tracked over different generations with insertion site-specific PCR. This study provided two stably inherited minichromosomes in oilseed rape and describes approaches to precisely characterize the truncation position and track the minichromosomes in offspring through multi-FISH, genome resequencing, and insertion site-specific PCR.
    Type of Medium: Online Resource
    ISSN: 1664-462X
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2021
    detail.hit.zdb_id: 2687947-5
    detail.hit.zdb_id: 2613694-6
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  • 5
    In: BMC Plant Biology, Springer Science and Business Media LLC, Vol. 21, No. 1 ( 2021-03-04)
    Abstract: Thinopyrum intermedium (2n = 6x = 42) is an important wild perennial Triticeae species exhibiting many potentially favorable traits for wheat improvement. Wheat- Th . intermedium partial amphiploids serve as a bridge to transfer desirable genes from Th . intermedium into common wheat. Results Three octoploid Trititrigia accessions (TE261–1, TE266–1, and TE346–1) with good resistances to stripe rust, powdery mildew and aphids were selected from hybrid progenies between Th . intermedium and the common wheat variety ‘Yannong 15’ (YN15). Genomic in situ hybridization (GISH), fluorescence in situ hybridization (FISH) and multicolor GISH (McGISH) analyses demonstrated that the three octoploid Trititrigia possess 42 wheat chromosomes and 14 Th. intermedium chromosomes. The 14 alien ( Th. intermedium ) chromosomes belong to a mixed genome consisting of J-, J S - and St-genome chromosomes rather than a single J, J S or St genome. Different types of chromosomal structural variation were also detected in the 1A, 6A, 6B, 2D and 7D chromosomes via FISH, McGISH and molecular marker analysis. The identity of the alien chromosomes and the variationes in the wheat chromosomes in the three Trititrigia octoploids were also different. Conclusions The wheat- Th. intermedium partial amphiploids possess 14 alien chromosomes which belong to a mixed genome consisting of J-, J S - and St- chromosomes, and 42 wheat chromosomes with different structural variations. These accessions could be used as genetic resources in wheat breeding for the transfer of disease and pest resistance genes from Th. intermedium to common wheat.
    Type of Medium: Online Resource
    ISSN: 1471-2229
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
    detail.hit.zdb_id: 2059868-3
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  • 6
    In: Genome, Canadian Science Publishing, Vol. 53, No. 5 ( 2010-05), p. 360-370
    Abstract: Heteromeric acetyl coenzyme A carboxylase (ACCase), a rate-limiting enzyme in fatty acid biosynthesis in dicots, is a multi-enzyme complex consisting of biotin carboxylase, biotin carboxyl carrier protein, and carboxyltransferase (α-CT and β-CT). In the present study, four genes encoding α-CT were cloned from Brassica napus , and two were cloned from each of the two parental species, B. rapa and B. oleracea . Comparative and cluster analyses indicated that these genes were divided into two major groups. The major divergence between group-1 and group-2 occurred in the second intron. Group-2 α-CT genes represented the ancestral form in the genus Brassica. The divergence of group-1 and group-2 genes occurred in their common ancestor 12.96–17.78 million years ago (MYA), soon after the divergence of Arabidopsis thaliana and Brassica (15–20 MYA). This time of divergence is identical to that reported for the paralogous subgenomes of diploid Brassica species (13–17 MYA). Real-time reverse transcription PCR revealed that the expression patterns of the two groups of genes were similar in different organs, except in leaves. To better understand the regulation and evolution of α-CT genes, promoter regions from two sets of orthologous gene copies from B. napus, B. rapa, and B. oleracea were cloned and compared. The function of the promoter of gene Bnα-CT-1-1 in group-1 and gene Bnα-CT-2-1 in group-2 was examined by assaying β-glucuronidase activity in transgenic A. thaliana. Our results will be helpful in elucidating the evolution and regulation of ACCase in oilseed rape.
    Type of Medium: Online Resource
    ISSN: 0831-2796 , 1480-3321
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 2010
    detail.hit.zdb_id: 2020635-5
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  • 7
    Online Resource
    Online Resource
    Elsevier BV ; 2013
    In:  Biochemical and Biophysical Research Communications Vol. 431, No. 4 ( 2013-02), p. 675-679
    In: Biochemical and Biophysical Research Communications, Elsevier BV, Vol. 431, No. 4 ( 2013-02), p. 675-679
    Type of Medium: Online Resource
    ISSN: 0006-291X
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2013
    detail.hit.zdb_id: 1461396-7
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  • 8
    In: Plant Breeding, Wiley, Vol. 135, No. 6 ( 2016-12), p. 751-758
    Abstract: Intermediate wheatgrass [ Thinopyrum intermedium (Host) Barkworth & D. R. Dewey] plant introductions ( PI ) have played a critical role in the development of improved intermediate wheatgrass cultivars. The objective of this study was to characterize a large number of intermediate wheatgrass populations over its native range for dry matter yield ( DMY ), crude protein ( CP ), in vitro true digestibility ( IVTD ), neutral detergent fibre ( NDF ), and rhizome development and genetic diversity and structure to identify superior populations and possible geographical regions in which to collect. Analysis of molecular variance using 643 AFLP bands partitioned 31% of the total genetic variation among these populations with 69% variance detected within populations. Bayesian cluster analysis identified two large groups designated as Asian and European under K  = 2. In general, European accessions had greater DMY than did Asian accessions. Observed trends were towards greater CP values in populations with Asian ancestry. Selection index values above zero were observed in populations with European ancestry, and the exception was the late‐maturing (208 days to bloom) populations with Asian ancestry. Plant populations 383 551, 383 561, 401 161, 401 173, 440 021, 578 692 (cv. Tegmar) and 598 740 had rhizome scores greater than 7.0. Despite significant differences detected between populations (Φ ST  = 0.3136; P  〈  0.001), there was strong indication of admixed co‐ancestry or possible gene flow between K  = 2–9 models.
    Type of Medium: Online Resource
    ISSN: 0179-9541 , 1439-0523
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2016
    detail.hit.zdb_id: 2020488-7
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  • 9
    In: BMC Plant Biology, Springer Science and Business Media LLC, Vol. 17, No. 1 ( 2017-12)
    Type of Medium: Online Resource
    ISSN: 1471-2229
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2017
    detail.hit.zdb_id: 2059868-3
    SSG: 12
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  • 10
    In: Genome, Canadian Science Publishing, Vol. 54, No. 3 ( 2011-03), p. 202-211
    Abstract: Comparative genomics is a useful tool to investigate gene and genome evolution. Biotin carboxylase (BC), an important subunit of heteromeric acetyl-CoA carboxylase (ACCase) that is a rate-limiting enzyme in fatty acid biosynthesis in dicots, catalyzes ATP, biotin carboxyl carrier protein, and CO 2 to form carboxybiotin carboxyl carrier protein. In this study, we cloned four genes encoding BC from Brassica napus L. (namely BnaC.BC.a, BnaC.BC.b, BnaA.BC.a, and BnaA.BC.b), and two were cloned from each of the two parental species Brassica rapa L. (BraA.BC.a and BraA.BC.b) and Brassica oleracea L. (BolC.BC.a and BolC.BC.b). Sequence analyses revealed that in B. napus the genes BnaC.BC.a and BnaC.BC.b were from the C genome of B. oleracea, whereas BnaA.BC.a and BnaA.BC.b were from the A genome of B. rapa. Comparative and cluster analysis indicated that these genes were divided into two major groups, BnaC.BC.a, BnaA.BC.a, BraA.BC.a, and BolC.BC.a in group-1 and BnaC.BC.b, BnaA.BC.b, BraA.BC.b, and BolC.BC.b in group-2. The divergence of group-1 and group-2 genes occurred in their common ancestor 13–17 million years ago (MYA), soon after the divergence of Arabidopsis and Brassica (15–20 MYA). This time of divergence is identical to the previously reported triplicated time of paralogous subgenomes of diploid Brassica species and the divergence date of group-1 and group-2 genes of α-carboxyltransferase, another subunit of heteromeric ACCase, in Brassica. Reverse transcription PCR revealed that the expression level of group-1 and group-2 genes varied in different organs, and the expression patterns of the two groups of genes were similar in different organs, except in flower. However, two paralogs of group-2 BC genes from B. napus could express differently in mature plants tested by generating BnaA.BC.b and BnaC.BC.b promoter–β-glucuronidase (GUS) fusions. The amino acid sequences of proteins encoded by these genes were highly conserved, except the sequence encoding predicted plastid transit peptides. The plastid transit peptides on the BC precursors of Brassica (71–72 amino acid residues) were predicted based on AtBC protein, compared, and confirmed by fusion with green fluorescent protein. Our results will be helpful in elucidating the evolution and the regulation of ACCase in the genus Brassica.
    Type of Medium: Online Resource
    ISSN: 0831-2796 , 1480-3321
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 2011
    detail.hit.zdb_id: 2020635-5
    SSG: 12
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