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. 2017 Jan 26;12(1):e0169820.
doi: 10.1371/journal.pone.0169820. eCollection 2017.

A Screen for Key Genes and Pathways Involved in High-Quality Brush Hair in the Yangtze River Delta White Goat

Affiliations

A Screen for Key Genes and Pathways Involved in High-Quality Brush Hair in the Yangtze River Delta White Goat

Haiyan Guo et al. PLoS One. .

Abstract

The Yangtze River Delta White Goat is the only goat breed that produces high-quality brush hair, or type III hair, which is specialized for use in top-grade writing brushes. There has been little research, especially molecular research, on the traits that result in high-quality brush hair in the Yangtze River Delta White Goat. To explore the molecular mechanisms of the formation of high-quality brush hair, High-throughput RNA-Seq technology was used to compare skin samples from Yangtze River Delta White Goats that produce high-quality hair and non high-quality hair for identification of the important genes and related pathways that might influence the hair quality traits. The results showed that 295 genes were expressed differentially between the goats with higher and lower hair quality, respectively. Of those genes, 132 were up-regulated, 62 were down-regulated, and 101 were expressed exclusively in the goats with high-quality brush hair. Gene Ontology and Metabolic Pathway Significant Enrichment analyses of the differentially expressed genes indicated that the MAP3K1, DUSP1, DUSP6 and the MAPK signaling pathway might play important roles in the traits important for high-quality brush hair.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. RNA sample integrity.
Note: Lanes 1–6 are samples A1, A2, A3, B1, B2, and B3, respectively.
Fig 2
Fig 2. eggNOG functional categories.
Fig 3
Fig 3. Pathway enrichment with differentially expressed genes.
Fig 4
Fig 4. The MAPK pathway.
Note: red tags showed the up-regulated genes, green tags showed the down-regulated genes.
Fig 5
Fig 5. Agarose gel electrophoresis of the PCR products.
Note: M: Marker I, 1: AOC3, 2: DUSP1, 3: VCL, 4: WNK1, 5: IGFBP1, 6: GAPDH, 7: S100A7
Fig 6
Fig 6. RT-qPCR dissociation curves of seven genes.
Note: A is AOC3, B is DUSP1, C is GAPDH, D is IGFBP, E is VCL, F is WNK1, and G is S100A7.
Fig 7
Fig 7. The relative expression of six genes.

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