Transcriptional profiling of the M. complexus in naked neck chickens suggest a direct pleiotropic effect of GDF7 on feathering and reduced hatchability.

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Alexander Charles Mott, Carina Blaschka, Andrea Mott, Clemens Falker-Gieske
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Abstract

Background: The locus for naked neck (Na) in chickens reduces feather coverage and leads to increased heat dissipation from the body surface resulting in better adaptability to hot conditions. However, the Na gene is linked to significantly lower hatchability due to an increased late embryonic mortality. It has been argued that the causative gene GDF7 may have a direct pleiotropic effect on hatchability via its effect on muscle development. Thus, the study presented here analyses the transcriptome of the hatching muscle (M. complexus) and shows how GDF7 impacts development leading to reduced hatching rates in Na chickens.

Results: Using 12 chicken embryos (6 x wildtype (Wt) and 6 x Na) RNA was extracted from the M. complexus of each embryo and sequenced. The resulting differential expression analyses led to the discovery of 461 differentially expressed (DE) genes in the M. complexus of the experimental group. Among those, 77 genes were of uncertain function (LOC symbols), with 31 were classified as uncharacterised. The regulation of a number of pathways involved in normal embryonic development, were found to be negatively influenced by the Na genotype. Further pathways involved in cell-cell adhesion, cell signalling pathways, and amino acid (AA) metabolism/transport were also observed. GDF7 (alias BMP12), whose localised overexpression in the neck skin causes the Na/Na phenotype, was significantly overexpressed in the M. complexus of Na/Na embryos, and shows a significant increase in the number of binding sites for the transcription factor PITX2 was also observed.

Conclusion: In Na chickens, GDF7 is under the control of a mutated cis-regulatory element, whose actions are known to suppress the development and distribution of feathers through the sensitizing action of retinoic acid. In this study, a number of DE genes with over 10 retinoic acid response elements (RAREs) in close proximity were observed, indicating changes to the retinol metabolism. With the understanding that the Na/Na mutation leads to increased retinoic acid activity, this indicates a high likelihood of GDF7 excerpting a direct pleiotropic effect, not just in the observed reduction in feather patterning, but also impacting the development of the M.complexus, and consequently leading to the reduced hatchability observed in birds with the Na/Na genotype. Furthermore, the enrichment of PITX2 binding sites in proximity to DE genes in the M. complexus, also indicates that muscle development is still ongoing in Na embryos. This suggests that the M. complexus is not yet fully developed, further increasing the potential for late embryonic mortality in Na chicks at hatching.

对裸颈鸡中的复合菌进行转录分析表明,GDF7 对羽毛生长和孵化率降低有直接的多效应。
背景:鸡的裸颈(Na)基因座可减少羽毛覆盖,增加体表散热,从而更好地适应炎热条件。然而,由于胚胎后期死亡率增加,Na 基因与孵化率显著降低有关。有观点认为,致病基因 GDF7 可能通过影响肌肉发育而对孵化率产生直接的多效应。因此,本研究分析了孵化肌肉(M. complexus)的转录组,并展示了 GDF7 如何影响发育导致 Na 鸡孵化率降低:使用 12 个鸡胚胎(6 个野生型(Wt)和 6 个 Na 型)从每个胚胎的复合肌中提取 RNA 并进行测序。通过差异表达分析,在实验组的复合体中发现了 461 个差异表达(DE)基因。其中 77 个基因功能不确定(LOC 符号),31 个基因未定性。研究发现,Na 基因型对一些涉及胚胎正常发育的通路的调控产生了负面影响。此外,还观察到涉及细胞-细胞粘附、细胞信号通路和氨基酸(AA)代谢/运输的其他通路。GDF7(别名 BMP12)在颈部皮肤的局部过表达会导致 Na/Na 表型,它在 Na/Na 胚胎的 M. complexus 中显著过表达,而且还观察到转录因子 PITX2 的结合位点数量显著增加:结论:在Na鸡体内,GDF7受一个突变的顺式调控元件控制,其作用是通过视黄酸的敏化作用抑制羽毛的发育和分布。在这项研究中,观察到一些 DE 基因与 10 多个视黄酸反应元件(RARE)非常接近,这表明视黄酸代谢发生了变化。由于 Na/Na 突变会导致视黄酸活性增加,这表明 GDF7 很可能会产生直接的多效应,不仅会导致观察到的羽毛花纹减少,还会影响 M.complexus 的发育,进而导致在 Na/Na 基因型鸟类中观察到的孵化率降低。此外,PITX2 结合位点在 M. 复合物中 DE 基因附近的富集也表明,Na 胚胎的肌肉发育仍在进行中。这表明 M. 复合体尚未完全发育,进一步增加了 Na 型雏鸟孵化时胚胎晚期死亡的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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