Yes-associated protein (YAP) and a transcriptional co-activator with PDZ-binding motif (TAZ) genes are crucial for regulating the size of mammalian tissues and organs as well as for many biological processes such as bone formation, cell lineage determination, tissue regeneration, and cell proliferation. The purpose of this study was to characterize the YAP and TAZ gene polymorphisms in 266 Guanzhong Dairy Goats and 299 Shanbei White Cashmere Goats and to explore their potential relationship with growth characteristics such as body weight and body length. After genotyping and using PCR amplification and Sanger sequencing to find polymorphisms in the YAP and TAZ genes, five InDels loci were found in the goat YAP gene and three InDels loci in the TAZ gene. The findings of the association analysis demonstrated that the goats' body weight, height, cannon circumference, chest depth, chest breadth, and chest circumference were all substantially influenced by five InDels loci in the YAP gene (p<0.05). Goat body height, trunk breadth, trunk length, body length, and body weight were all substantially impacted by three InDels loci in the TAZ gene (p<0.05). In conclusion, eight InDels loci of goat YAP and TAZ were found in this study, and their impacts on goat phenotype were disclosed. These results might offer fresh avenues for boosting goat molecular breeding.
为探究獭兔和伊高乐肉兔杂交后代生长发育的规律,并为其杂种后代的选种选配和饲养管理提供科学依据,实验选用獭兔和伊高乐肉兔作为亲本,测定正反交F1 代的体重和体尺,并利用Logistic、Gompertz和Von Bertallanffy模型拟合正反交后代 0~17 周龄的生长曲线.结果表明:獭肉杂交(TR组)在 75 日龄、90 日龄及 120 日龄的体重均高于肉獭杂交(RT组)(P<0.05),在 11 周龄后 2 组体重增长趋势开始发生变化,TR组生长速度相比RT组更快;Logistic、Gompertz和Von Bertallanffy模型对正反交F1 代体重均具有较高的拟合度(R2>0.993),其中Logistic模型对正反交后代的拟合效果最佳;在 120 日龄时,TR组与RT组的胸围差异显著,2 组体尺的生长模型拟合度均在 0.978 以上.研究结果可为獭兔和肉兔的杂交利用提供理论依据.
N6-methyladenosine (m6A), the most abundant internal mRNA modification in eukaryotes, plays a vital role in regulating adipogenesis. However, its underlying mechanism remains largely unknown. Our previous study found that ADRB1 gene has m6A modification in both muscle and fat tissue. In this study, we interfered with FTO and ADRB1 genes After we cultured rabbit preadipocytes respectively. Oil red O staining and triglyceride assay were used to detect adipocyte differentiation. RT-qPCR was used to detect gene expression level and MeRIP-qPCR was used to detect the m6A modification level of gene. The results showed that FTO promoted the differentiation of adipocytes. At the same time, FTO up regulated the expression of ADRB1 gene and down regulated the m6A modification level of ADRB1 gene. Finally, we found that ADRB1 inhibited adipocyte differentiation. Together, we showed that FTO promoted adipocyte differentiation by regulating ADRB1 gene through m6A modification.
哺乳动物触发促性腺激素释放激素分泌的类型分为两类:自发排卵或诱导排卵.在前一种情况下,成熟卵泡产生的卵巢类固醇引起下丘脑释放促性腺激素释放激素,但在后一种情况下,促性腺激素释放激素的分泌需要交配等刺激.目前,对刺激性排卵的相关研究报道较少.该文主要以非自发排卵动物为研究对象,阐述刺激性排卵方面的相关进展,并对其机制进行进一步的探讨.
N6-methyladenosine (m6A) is the most prevalent internal form of modification in messenger RNA in higher eukaryotes and plays an important role in cancer, immunity, reproduction, development, and fat deposition. Intramuscular fat is the main factor used to measure the meat quality of an animal. The deposition of intramuscular fat and perirenal fat increases with age. However, there is no data on m6A modification of Rex rabbits and its potential biological roles in adipose deposition and muscle growth. Here, we performed two high-throughput sequencing methods, m6A-modified RNA immunoprecipitation sequence (MeRIP-seq) and RNA sequence (RNA-seq), to identify key genes with m6A modification on fat deposition in the muscle and adipose tissues of Rex rabbits. Then, qRT-PCR was used to identify the differently methylated genes related to fat deposition. Our findings showed that there were 12,876 and 10,973 m6A peaks in the rabbit muscle and adipose tissue transcriptomes, respectively. Stop codons, 3′-untranslated regions, and coding regions were found to be mainly enriched for m6A peaks. In addition, we found 5 differential methylases and 12 key genes of methylation modification related to fat deposition between muscle and adipose tissues samples. The expression levels of six random key genes were significantly higher in the fat than that in the muscle of Rex rabbits at different stages (p < 0.01). Finally, five differential methylases were found to regulate adipogenesis by affecting the expression of screened genes in different ways. These findings provided a theoretical basis for our future research on the function of m6A modification during the growth of fat deposits.