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Simple Summary Fertility is one of the essential reproduction traits of bulls, and accurate prediction of fertility potential using a semen sample from a donor bull for artificial insemination is crucial to achieve consistently high reproductive efficiency. Somatic cells, such as Sertoli cells and Leydig cells, are important in testis formation and provide a nurturing and regulatory environment for spermatogenesis. Furthermore, it was suggested that non-coding RNAs, such as microRNAs, long non-coding RNAs, circular RNAs, and Piwi-interacting RNA, function as important regulators of gene expression at post-transcriptional level in spermatogenesis. In this study, microRNA-34c was verified to specifically regulate the AXL gene by targeting a sequence in the 3’ UTR; miRNA-34c can also influence the proliferation, apoptosis, and relative abundance of the transcript of male-reproduction-related genes. Therefore, microRNA-34c can be considered an essential regulator in the process of bull spermatogenesis. These results identify a key microRNA and functional genes in the process of cattle male reproduction, providing useful information for future marker-assisted selection of bulls with excellent sperm quality. Abstract MicroRNAs (miRNAs) play significant roles in mammalian spermatogenesis. Sertoli cells can provide a stable microenvironment and nutritional factors for germ cells, thus playing a vital role in spermatogenesis. However, few studies elucidate the regulation of bovine testicular Sertoli cells by miRNAs. Here, we have reported that miRNA-34c (miR-34c) regulates proliferation, apoptosis, and relative transcripts abundance gene in bovine Sertoli cells. In bovine Sertoli cells, overexpression of miR-34c inhibited proliferation and relative abundance of gene transcripts while promoting apoptosis of Sertoli cells, and the effects were the opposite when miR-34c was knocked down. Receptor tyrosine kinase (AXL) was identified as a direct target gene of miR-34c in Sertoli cells, validated by analysis of the relative abundance of AXL transcript and dual-luciferase reporter assay. The relative abundance of the transcript of genes related to male reproduction in Sertoli cells was changed after the AXL gene was overexpressed, as demonstrated by the RT2 Profiler PCR Array results. In summary, miR-34c specifically regulated the AXL gene by targeting a sequence in the 3′-UTR, which could influence proliferation, apoptosis, and relative abundance of the transcript of male reproduction-related genes. Therefore, miR-34c could be considered an essential regulator in the process of bull spermatogenesis.

In this study, we precisely constructed and transfected the overexpression and interference vectors in BFFs to evaluate the role of DLK1 gene on lipid metabolism in vitro. The expression of of DLK1 in the mRNA and protein level tended to reduce, and TGs were significantly increased in the pGPU6-shDLK1 group compared to the control group (p &lt, 0.05). The expression of DLK1 in the mRNA and protein level were increased in the pBI-CMV3-DLK1 group compared to the control group, and the TGs content showed a significant decrease in the pBI-CMV3-DLK1 group (p &lt, 0.05). Meanwhile, we used the restriction fragment length polymorphism (RFLP-PCR) detection method to screen SNPs further to explore and analyze the relationship between the gene and the economic traits of 28-month-old Chinese Simmental and the fatty acids composition of cattle longissimus muscle. The result showed that two SNPs, IVS3 + 478 C&gt, T and IVS3 + 609 T&gt, G, were identified as being significantly associated with carcass and meat quality traits in Chinese Simmental, such as the carcass fat coverage rate, loin eye muscle area, and fat color score. In summary, our results indicated that DLK1 can affect lipid metabolism in bovine and these two SNPs might be applied as genetic markers of meat quality traits for beef cattle breeding.

Epiphytic bryophytes are known to perform essential ecosystem functions, but their sensitivity to environmental quality and change makes their survival and development vulnerable to global changes, especially habitat loss in urban environments. Fortunately, extensive urban tree planting programs worldwide have had a positive effect on the colonization and development of epiphytic bryophytes. However, how epiphytic bryophytes occur and grow on planted trees remain poorly known, especially in urban environments. In the present study, we surveyed the distribution of epiphytic bryophytes on tree trunks in a Schima superba Gardn. et Champ. urban plantation and then developed count data models, including tree characteristics, stand characteristics, human disturbance, terrain factors, and microclimate to predict the drivers on epiphytic bryophyte recruitment. Different counting models (Poisson, Negative binomial, Zero-inflated Poisson, Zero-inflated negative binomial, Hurdle-Poisson, Hurdle-negative binomial) were compared for a data analysis to account for the zero-inflated data structure. Our results show that (i) the shaded side and base of tree trunks were the preferred locations for bryophytes to colonize in urban plantations, (ii) both hurdle models performed well in modeling epiphytic bryophyte recruitment, and (iii) both hurdle models showed that the tree height, diameter at breast height (DBH), leaf area index (LAI), and altitude (ALT) promoted the occurrence of epiphytic bryophytes, but the height under branch and interference intensity of human activities opposed the occurrence of epiphytic bryophytes. Specifically, DBH and LAI had positive effects on the species richness recruitment count, similarly, DBH and ALT had positive effects on the abundance recruitment count, but slope had a negative effect. To promote the occurrence and growth of epiphytic bryophytes in urban tree planting programs, we suggest that managers regulate suitable habitats by cultivating and protecting large trees, promoting canopy closure, and controlling human disturbance.