scholarly journals Transcriptome Analysis of Orange Head Chinese Cabbage (Brassica rapaL. ssp.pekinensis) and Molecular Marker Development

2017 ◽  
Vol 2017 ◽  
pp. 1-8 ◽  
Author(s):  
Jingjuan Li ◽  
Yihui Zhang ◽  
Qian Ding ◽  
Huayin Li ◽  
Lifeng Liu ◽  
...  
Keyword(s):  
Chinese Cabbage ◽  
Carotenoid Biosynthesis ◽  
Underlying Mechanism ◽  
Indel Marker ◽  
Carotenoid Content ◽  
Nucleotide Polymorphisms ◽  
Visual Appearance ◽  
Carotenoid Biosynthesis Pathway ◽  
Molecular Marker Development ◽  
Pigment Accumulation

Due to the visual appearance and high carotenoid content, orange inner leaves are a desirable trait for the Chinese cabbage. To understand the molecular mechanism underlying the formation of orange inner leaves, theBrCRTISO(Bra031539) gene, as theBr-orcandidate gene, was analyzed among the white and orange varieties, and 7 single nucleotide polymorphisms (SNPs) were identified. However, only one SNP (C952to T952) altered the amino acid sequence, resulting in a mutation from Leu318to Phe318in the orange varieties. Additionally, we analyzed differentially expressed genes (DEGs) between the orange and white F2individuals (14-401 × 14-490) and found four downregulated genes were involved in the carotenoid biosynthesis pathway, which may lead to the accumulation of prolycopene and other carotenoid pigments in the orange inner leaves. In addition, we developed a novel InDel marker in the first intron, which cosegregates with the phenotypes of orange color inner leaves. In conclusion, these findings enhance our understanding of the underlying mechanism of pigment accumulation in the inner leaves of the Chinese cabbage. Additionally, the SNP (C952to T952) and the InDel marker will facilitate the marker-assisted selection during Chinese cabbage breeding.

scholarly journals Comparative transcriptomic analysis reveals a series of single nucleotide polymorphism between red- and white-fleshed loquats (Eriobotrya japonica)

2017 ◽  
Vol 53 (No. 3) ◽  
pp. 97-106
Author(s):  
S. Sun ◽  
J. Li ◽  
D. Chen ◽  
H. Xie ◽  
M. Tu ◽  
...  
Keyword(s):  
Developmental Stages ◽  
De Novo ◽  
Average Length ◽  
Carotenoid Biosynthesis ◽  
Expression Level ◽  
Eriobotrya Japonica ◽  
Carotenoid Content ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide ◽  
Fruit Samples

Loquat (Eriobotrya japonica) is an economically important crop and red-fleshed cultivars have a much higher carotenoid content than white-fleshed cultivars. We used Illumina RNA-seq technology to gain a global overview of the loquat transcriptome from a mixture of fruit samples at different developmental stages for both red-fleshed and white-fleshed loquat. A total of 94.98 million paired-end short reads were obtained and 61 586 unigenes were generated from de novo assembly with an average length of 817 bp. Among these unigenes, 44 710 unigenes were annotated by blast against Nr, Swissprot, GO, COG and KEGG databases. For these annotated unigenes, 123 biosynthesis pathways were predicted by mapping these unigenes to the reference canonical pathways and 41 unigenes were predicted to be involved in carotenoid biosynthesis. RT-qPCR analysis showed that the expression level of the LCYB gene was higher in red-fleshed loquat and the CRTRB gene had a higher expression level in white-fleshed loquat. Comparative analysis of the two transcriptomes revealed 2396 single nucleotide polymorphisms (SNPs) between red- and white-fleshed loquats. The majority of SNPs identified between the two loquat cultivars were nonsense mutations and one out of eleven SNPs in candidate genes involved in carotenoid biosynthesis was a sense mutation. This suggests that the analysis based on transcriptomes can reveal key genes related to the carotenoid biosynthesis and more carotene in red-fleshed loquat cultivars may result from both more carotene produced by the higher expression of LCYB genes and less carotene converted because of the low expression of the CRTRB gene. All these results from the transcriptome analysis will be useful for the elucidation of genetic differences between red- and white-fleshed loquat fruits and further functional analysis for genes responsible for carotenoid accumulation.  

scholarly journals Changes in Fruit pigment accumulation, chloroplast development, and Transcriptome analysis in the CRISPR/Cas9-Mediated Knockout of Stay-green 1 (slsgr1) Mutant

2021 ◽  
Author(s):  
Liqun Ma ◽  
Ni Zeng ◽  
Ke Cheng ◽  
Jinyan Li ◽  
Keru Wang ◽  
...  
Keyword(s):  
Color Change ◽  
Tomato Fruit ◽  
Carotenoid Biosynthesis ◽  
Carotenoid Content ◽  
Rna Seq ◽  
Loss Of Function ◽  
Stay Green ◽  
Pigment Accumulation ◽  
Brown Color

Abstract The tomato fruit of green-flesh (gf) mutant ripen to a muddy brown color and has been demonstrated previously to be a loss-of-function mutant. Here, we provide more evidence to support this view that SlSGR1 involved in color change in ripening tomato fruits. Knocking out SlSGR1 expression using a clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 genome editing strategy showed obviously a muddy brown color with significantly higher chlorophyll and carotenoid content compared with WT fruits. To further verify the role of SlSGR1 in fruit color change, we performed RNA-seq analysis, where a total of 354 differentially expressed genes (124/230 down-/upregulated) were identified between WT and slsgr1. Additionally, the expression of numerous genes associated with photosynthesis and chloroplast function changed significantly when SlSGR1 was knocked out. Taken together, these results indicate that SlSGR1 is involved color change in ripening fruit via chlorophyll degradation and carotenoid biosynthesis.

scholarly journals An apple (Malus domestica) AP2/ERF transcription factor modulates carotenoid accumulation

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Qingyuan Dang ◽  
Haiyun Sha ◽  
Jiyun Nie ◽  
Yongzhang Wang ◽  
Yongbing Yuan ◽  
...  
Keyword(s):  
Transcription Factor ◽  
Malus Domestica ◽  
Carotenoid Biosynthesis ◽  
Carotenoid Content ◽  
Ethylene Response Factor ◽  
Biosynthesis Pathway ◽  
Carotenoid Accumulation ◽  
Carotenoid Biosynthesis Pathway ◽  
Β Carotene ◽  
Erf Transcription Factor

AbstractColor is an important trait for horticultural crops. Carotenoids are one of the main pigments for coloration and have important implications for photosynthesis in plants and benefits for human health. Here, we identified an APETALA2 (AP2)/ETHYLENE RESPONSE FACTOR (ERF) transcription factor named MdAP2-34 in apple (Malus domestica Borkh.). MdAP2-34 expression exhibited a close correlation with carotenoid content in ‘Benin Shogun’ and ‘Yanfu 3’ fruit flesh. MdAP2-34 promotes carotenoid accumulation in MdAP2-34-OVX transgenic apple calli and fruits by participating in the carotenoid biosynthesis pathway. The major carotenoid contents of phytoene and β-carotene were much higher in overexpressing MdAP2-34 transgenic calli and fruit skin, yet the predominant compound of lutein showed no obvious difference, indicating that MdAP2-34 regulates phytoene and β-carotene accumulation but not lutein. MdPSY2-1 (phytoene synthase 2) is a major gene in the carotenoid biosynthesis pathway in apple fruit, and the MdPSY2-1 gene is directly bound and transcriptionally activated by MdAP2-34. In addition, overexpressing MdPSY2-1 in apple calli mainly increases phytoene and total carotenoid contents. Our findings will advance and extend our understanding of the complex molecular mechanisms of carotenoid biosynthesis in apple, and this research is valuable for accelerating the apple breeding process.

scholarly journals Genetic Characterization of the Carotenoid Biosynthetic Pathway in Methylobacterium extorquens AM1 and Isolation of a Colorless Mutant

2003 ◽  
Vol 69 (12) ◽  
pp. 7563-7566 ◽  
Author(s):  
Stephen J. Van Dien ◽  
Christopher J. Marx ◽  
Brooke N. O'Brien ◽  
Mary E. Lidstrom
Keyword(s):  
Biosynthetic Pathway ◽  
Genetic Characterization ◽  
Carotenoid Biosynthesis ◽  
Biosynthesis Pathway ◽  
Wild Type ◽  
Methylobacterium Extorquens ◽  
Growth Properties ◽  
Carotenoid Biosynthesis Pathway ◽  
Free Strain

ABSTRACT Genomic searches were used to reconstruct the putative carotenoid biosynthesis pathway in the pink-pigmented facultative methylotroph Methylobacterium extorquens AM1. Four genes for putative phytoene desaturases were identified. A colorless mutant was obtained by transposon mutagenesis, and the insertion was shown to be in one of the putative phytoene desaturase genes. Mutations in the other three did not affect color. The tetracycline marker was removed from the original transposon mutant, resulting in a pigment-free strain with wild-type growth properties useful as a tool for future experiments.

scholarly journals Transcriptome Sequencing and Biochemical Analysis of Perianths and Coronas Reveal Flower Color Formation in Narcissus pseudonarcissus

2018 ◽  
Vol 19 (12) ◽  
pp. 4006 ◽  
Author(s):  
Xi Li ◽  
Dongqin Tang ◽  
Hui Du ◽  
Yimin Shi
Keyword(s):  
Flower Color ◽  
Carotenoid Biosynthesis ◽  
Carotenoid Content ◽  
Rna Seq ◽  
Color Formation ◽  
Light Yellow ◽  
Color Fading ◽  
Narcissus Pseudonarcissus ◽  
Bulbous Plant ◽  
Β Carotene

Narcissus pseudonarcissus is an important bulbous plant with white or yellow perianths and light yellow to orange-red coronas, but little is known regarding the biochemical and molecular basis related to flower color polymorphisms. To investigate the mechanism of color formation, RNA-Seq of flower of two widely cultured cultivars (‘Slim Whitman’ and ‘Pinza’) with different flower color was performed. A total of 84,463 unigenes were generated from the perianths and coronas. By parallel metabolomic and transcriptomic analyses, we provide an overview of carotenoid biosynthesis, degradation, and accumulation in N. pseudonarcissus. The results showed that the content of carotenoids in the corona was higher than that in the perianth in both cultivars. Accordingly, phytoene synthase (PSY) transcripts have a higher abundance in the coronas than that in perianths. While the expression levels of carotenoid biosynthetic genes, like GGPPS, PSY, and LCY-e, were not significantly different between two cultivars. In contrast, the carotenoid degradation gene NpCCD4 was highly expressed in white-perianth cultivars, but was hardly detected in yellow-perianth cultivars. Silencing of NpCCD4 resulted in a significant increase in carotenoid accumulation, especially in all-trans-β-carotene. Therefore, we presume that NpCCD4 is a crucial factor that causes the low carotenoid content and color fading phenomenon of ‘Slim Whitman’ by mediating carotenoid turnover. Our findings provide mass RNA-seq data and new insights into carotenoid metabolism in N. pseudonarcissus.

scholarly journals EPR study of thylakoid membrane dynamics in mutants of the carotenoid biosynthesis pathway of Synechocystis sp. PCC6803.

2012 ◽  
Vol 59 (1) ◽  
Author(s):  
Kinga Kłodawska ◽  
Przemysław Malec ◽  
Mihály Kis ◽  
Zoltán Gombos ◽  
Kazimierz Strzałka
Keyword(s):  
Optimal Growth ◽  
Carotenoid Biosynthesis ◽  
Growth Conditions ◽  
Thylakoid Membranes ◽  
Membrane Dynamics ◽  
Biosynthesis Pathway ◽  
Light Regimes ◽  
Genes Encoding ◽  
Splitting Parameter ◽  
Carotenoid Biosynthesis Pathway

EPR spectroscopy using 5-doxylstearic acid (5-SASL) and 16-doxylstearic acid (16-SASL) spin probes was used to study the fluidity of thylakoid membranes. These were isolated from wild type Synechocystis and from several mutants in genes encoding selected enzymes of the carotenoid biosynthesis pathway and/or acyl-lipid desaturases. Cyanobacteria were cultivated at 25°C and 35°C under different light regimes: photoautotrophically (PAG) and/or in light-activated heterotrophic conditions (LAHG). The relative fluidity of membranes was estimated from EPR spectra based on the empirical outermost splitting parameter in a temperature range from 15°C to 40°C. Our findings demonstrate that in native thylakoid membranes the elimination of xanthophylls decreased fluidity in the inner membrane region under optimal growth conditions (25°C) and increased it under sublethal heat stress (35°C). This indicated that the overall fluidity of native photosynthetic membranes in cyanobacteria may be influenced by the ratio of polar to non-polar carotenoid pools under different environmental conditions.

scholarly journals Transcriptome dynamics underlying flower color in marigold (Tagetes erecta L.)

2019 ◽  
Author(s):  
Huali Zhang ◽  
Shiya Zhang ◽  
Hua Zhang ◽  
Xi Chen ◽  
Fang Liang ◽  
...  
Keyword(s):  
Inbred Line ◽  
Developmental Stages ◽  
De Novo ◽  
Flower Color ◽  
Carotenoid Biosynthesis ◽  
Cdna Libraries ◽  
Carotenoid Content ◽  
Tagetes Erecta ◽  
Tagetes Erecta L ◽  
Carotenoid Degradation

Abstract Background: Marigold (Tagetes erecta L.) is an important ornamental plant with a wide variety of flower colors. Despite its economic value, few biochemical and molecular studies have explored the generation of flower color in this species. Results: To study the mechanism underlying marigold petal color, we performed a metabolomics analysis and de novo cDNA sequencing on the inbred line ‘V-01’ and its petal color mutant ‘V-01M’ at four flower developmental stages. A total of 49,217 unigenes were identified from 24 cDNA libraries. Based on our transcriptomic and metabolomic analyses, we present an overview of carotenoid biosynthesis, degradation, and accumulation in marigold flowers. The carotenoid content of the yellow mutant ‘V-01M’ was higher than that of the orange inbred line ‘V-01’, and the abundances of the yellow compounds lutein, neoxanthin, violaxanthin, zeaxanthin, and antheraxanthin were significantly higher in the mutant. During flower development, the carotenoid biosynthesis genes were upregulated in both ‘V-01’ and ‘V-01M’, with no significant differences between the two lines. By contrast, the carotenoid degradation genes were dramatically downregulated in the yellow mutant ‘V-01M’. Conclusions: We therefore speculate that the carotenoid degradation genes are the key factors regulating the carotenoid content of marigold flowers. Our research provides a large amount of transcriptomic data and insights into the marigold color metabolome.

scholarly journals Inheritance Pattern and Molecular Markers for Resistance to Blackleg Disease in Cabbage

Plants ◽  
2019 ◽  
Vol 8 (12) ◽  
pp. 583
Author(s):  
Mostari Jahan Ferdous ◽  
Mohammad Rashed Hossain ◽  
Jong-In Park ◽  
Arif Hasan Khan Robin ◽  
Denison Michael Immanuel Jesse ◽  
...  
Keyword(s):  
Molecular Markers ◽  
High Resolution Melting ◽  
Leptosphaeria Maculans ◽  
Inbred Lines ◽  
Indel Marker ◽  
Detection Accuracy ◽  
Nucleotide Polymorphisms ◽  
Blackleg Disease ◽  
Marker Assisted Breeding ◽  
Single Nucleotide

The inheritance and causal loci for resistance to blackleg, a devastating disease of Brassicaceous crops, are yet to be known in cabbage (Brassica oleracea L.). Here, we report the pattern of inheritance and linked molecular marker for this trait. A segregating BC1 population consisting of 253 plants was raised from resistant and susceptible parents, L29 (♀) and L16 (♂), respectively. Cotyledon resistance bioassay of BC1 population, measured based on a scale of 0–9 at 12 days after inoculation with Leptosphaeria maculans isolate 03–02 s, revealed the segregation of resistance and ratio, indicative of dominant monogenic control of the trait. Investigation of potential polymorphism in the previously identified differentially expressed genes within the collinear region of ‘B. napus blackleg resistant loci Rlm1′ in B. oleracea identified two insertion/deletion (InDel) mutations in the intron and numerous single nucleotide polymorphisms (SNPs) throughout the LRR-RLK gene Bol040029, of which six SNPs in the first exon caused the loss of two LRR domains in the susceptible line. An InDel marker, BLR-C-InDel based on the InDel mutations, and a high resolution melting (HRM) marker, BLR-C-2808 based on the SNP C2808T in the second exon were developed, which predicated the resistance status of the BC1 population with 80.24%, and of 24 commercial inbred lines with 100% detection accuracy. This is the first report of inheritance and molecular markers linked with blackleg resistance in cabbage. This study will enhance our understanding of the trait, and will be helpful in marker assisted breeding aiming at developing resistant cabbage varieties.

Molecular genetics of the carotenoid biosynthesis pathway in plants and algae

1997 ◽  
Vol 69 (10) ◽  
pp. 2151-2158 ◽  
Author(s):  
Joseph Hirschberg ◽  
M. Cohen ◽  
Mark Harker ◽  
Tamar Lotan ◽  
Varda Mann ◽  
...  
Keyword(s):  
Molecular Genetics ◽  
Carotenoid Biosynthesis ◽  
Biosynthesis Pathway ◽  
Carotenoid Biosynthesis Pathway
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