Genetic and Transcription Profile Analysis of Tissue-Specific Anthocyanin Pigmentation in Carrot Root Phloem

被引:14
作者
Bannoud, Florencia [1 ]
Carvajal, Sofia [1 ]
Ellison, Shelby [2 ]
Senalik, Douglas [3 ]
Gomez Talquenca, Sebastian [4 ]
Iorizzo, Massimo [5 ,6 ]
Simon, Philipp W. [2 ,3 ]
Cavagnaro, Pablo F. [1 ,7 ,8 ]
机构
[1] Consejo Nacl Invest Cient & Tecn CONICET, Av Rivadavia 1917,C1033, Buenos Aires, DF, Argentina
[2] Univ Wisconsin Madison, Dept Hort, 1575 Linden Dr, Madison, WI 53706 USA
[3] Univ Wisconsin Madison, USDA ARS, Vegetable Crops Res Unit, 1575 Linden Dr, Madison, WI 53706 USA
[4] Instituto Nacl Tecnol Agropecuaria INTA EEA Mendo, San Martin 3853,M5507, Mendoza, Argentina
[5] North Carolina State Univ, Plants Human Hlth Inst, Kannapolis, NC 28081 USA
[6] N Carolina State Univ, Dept Hort Sci, Raleigh, NC 27695 USA
[7] Inst Nacl Tecnol Agropecuaria INTA, EEA Consulta, Ex Ruta 40 Km 96,M5567, Mendoza, Argentina
[8] Univ Nacl Cuyo, Fac Ciencias Agrarias, Inst Horticultura, M5528, Mendoza, Argentina
关键词
Daucus carota; anthocyanin; phloem pigmentation; genetic mapping; RNA-Seq; candidate genes; RT-qPCR; DIFFERENTIAL EXPRESSION ANALYSIS; BIOSYNTHESIS; ACCUMULATION; ARABIDOPSIS; COLOR;
D O I
10.3390/genes12101464
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In purple carrots, anthocyanin pigmentation can be expressed in the entire root, or it can display tissue specific-patterns. Within the phloem, purple pigmentation can be found in the outer phloem (OP) (also called the cortex) and inner phloem (IP), or it can be confined exclusively to the OP. In this work, the genetic control underlying tissue-specific anthocyanin pigmentation in the carrot root OP and IP tissues was investigated by means of linkage mapping and transcriptome (RNA-seq) and phylogenetic analyses; followed by gene expression (RT-qPCR) evaluations in two genetic backgrounds, an F-2 population (3242) and the inbred B7262. Genetic mapping of 'root outer phloem anthocyanin pigmentation' (ROPAP) and inner phloem pigmentation (RIPAP) revealed colocalization of ROPAP with the P-1 and P-3 genomic regions previously known to condition pigmentation in different genetic stocks, whereas RIPAP co-localized with P-3 only. Transcriptome analysis of purple OP (POP) vs. non-purple IP (NPIP) tissues, along with linkage and phylogenetic data, allowed an initial identification of 28 candidate genes, 19 of which were further evaluated by RT-qPCR in independent root samples of 3242 and B7262, revealing 15 genes consistently upregulated in the POP in both genetic backgrounds, and two genes upregulated in the POP in specific backgrounds. These include seven transcription factors, seven anthocyanin structural genes, and two genes involved in cellular transport. Altogether, our results point at DcMYB7, DcMYB113, and a MADS-box (DCAR_010757) as the main candidate genes conditioning ROPAP in 3242, whereas DcMYB7 and MADS-box condition RIPAP in this background. In 7262, DcMYB113 conditions ROPAP.</p>
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页数:20
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