Transcriptome analysis of cattle embryos based on single cell RNA-seq | [Pakistan Journal of Zoology • 2023]

Author(s):

1. Jie Wang: College of Life Sciences, Tarim University, Alar, Xinjiang 843300, China

2. Di Fang: College of Life Sciences, Tarim University, Alar, Xinjiang 843300, China

3. Jianqing Zhao: College of Life Sciences, Tarim University, Alar, Xinjiang 843300, China

4. Fei Huang: College of Animal Science, Tarim University, Alar, Xinjiang 843300, China

5. Bo Liu: College of Animal Science, Tarim University, Alar, Xinjiang 843300, China

6. Weikun Tao: College of Animal Science, Tarim University, Alar, Xinjiang 843300, China

7. Baoshan Cui: College of Animal Science, Tarim University, Alar, Xinjiang 843300, China

8. Qinghua Gao: College of Life Sciences, Tarim University, Alar, Xinjiang 843300, China; College of Animal Science, Tarim University, Alar, Xinjiang 843300, China; Key Laboratory of Tarim Animal Husbandry Science and Technology, Xinjiang Production and Construction Corps, Alar, Xinjiang 843300, China

Abstract:

Over the past few years, transcriptome sequencing has been applied to livestock and poultry, helping to select and investigate candidate genes associated with important traits. Yet, so far, only a few studies have reported diferences in single-cell transcriptome between bovine embryos of diferent genders. In this study, we performed transcriptome analysis of cattle embryos based on a single Cell RNA-Seq. Bovine sex-controlled semen for artificial insemination were used to obtain diferent stage embryos: bovine 8 cell XX embryo, 8 cell XY embryo, 16 cell XX embryo, 16 cell XY embryo, morula XX embryo, morula XY embryo, blastocyst XX embryo, and blastocyst XY embryo. A sequencing library was constructed by the Smart-Seq2 amplification. The transcriptome was sequenced by Illumina HiSeqXten high-throughput sequence technology, and efective sequences were analyzed by functional annotation and related bioinformatics analysis. We found that Q30 percentage range of eight samples was 91.7992.37%. The filtration sequence was 44106250-54234844. Compared with the reference genome by TopHat software, the net reading ratio of the bovine reference gene at each stage was 93.17-9 4.23%, the ratio of sequence numbers to multiple sites of the genome was 2.99-4.89. The DEG was identified by using the fold change =2 and FDR <0.01 as cut-of values. There were 525 diferentially expressed genes. GO and KEGG analysis showed that “cell part”, “organelle”, and organelle part” were significantly enriched in cell composition categories. As for molecular functional categories, DEGs were significantly enriched in cellular process “,” biological regulation “and metabolic process” during biological processes. Moreover, KEGG analysis showed that the most abundant pathways were oxidative phosphorylation and Wnt signaling pathway”,”MAPK signaling pathway “,” Regulation of actin cytoskeleton “and VEGF signaling pathway”. To conclude, these RNA-Seq results confirmed the diferential expression of several genes in embryos of diferent genders during embryonic development. These DEGs partcipate in the transcriptional regulation of bovine embryonic development of diferent genders.

Page(s): 1865-1872

DOI: 10.17582/journal.pjz/20211016091046

Published: Journal: Pakistan Journal of Zoology, Volume: 55, Issue: 4, Year: 2023

Keywords:

Cattle , RNASeq , XXXY embryo , Early embryo , Diferential expression

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