Screening of reliable reference genes for the normalization of RT-qPCR in chicken oviduct tract

被引:0
|
作者
Shu, Xin [1 ,2 ]
Hua, Guoying [3 ]
Zheng, Xiaotong [1 ,2 ]
Chen, Ziwei [1 ,2 ]
Zhang, Jilong [1 ]
Zhuang, Wuchao [1 ]
Chen, Jianfei [1 ,2 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Biotechnol, Jiangsu Key Lab Sericultural Biol & Anim Biotechno, Zhenjiang 212100, Peoples R China
[2] Chinese Acad Agr Sci, Sericultural Sci Res Ctr, Key Lab Silkworm & Mulberry Genet Improvement, Minist Agr & Rural Affairs, Zhenjiang 212100, Peoples R China
[3] Chinese Acad Agr Sci, Agr Genom Inst Shenzhen, Shenzhen Branch, Guangdong Lab Lingnan Modern Agr, Shenzhen 518120, Peoples R China
关键词
chicken; RT-qPCR; stable reference gene; RNA-seq; oviduct; HOUSEKEEPING GENES; BETA-ACTIN; PCR DATA; EXPRESSION; GAPDH;
D O I
10.1016/j.psj.2024.103980
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Utilizing publicly available RNA-seq data to screen for ideal reference genes is more efficient and accurate than traditional methods. Previous studies have identified optimal reference genes in various chicken tissues, but none have specifically focused on the oviduct (including the infundibulum, magnum, isthmus, uterus, and vagina), which is crucial for egg production. Identifying stable reference genes in the oviduct is essential for improving research on gene expression levels. This study investigated genes with consistent expression patterns in the chicken oviduct, encompassing both individual oviduct tract tissues and the entire oviduct, by utilizing multiple RNA-seq datasets. The screening results revealed the discovery of 100 novel reference genes in each segment of oviduct tissues, primarily associated with cell cycle regulation and RNA binding. Moreover, the majority of housekeeping genes ( HKGs ) showed inconsistent expression levels across distinct samples, suggesting their lack of stability under varying conditions. The stability of the newly identified reference genes was assessed in comparison to previously validated stable reference genes in chicken oviduct and commonly utilized HKGs, employing traditional reference gene screening methods. HERPUD2, CSDE1, VPS35, PBRM1, LSM14A , and YWHAB were identified to be suitable novel reference gene for different parts of the oviduct. HERPUD2 and YWHAB were reliable for gene expression normalization throughout the oviduct tract. Furthermore, overexpression and interference assays in DF1 cells showed LSM14A and YWHAB play a crucial role in cell proliferation, highlighting the importance of these newly reference genes for further research. Overall, this study has expanded the options for reference genes in RT-qPCR experiments in different segments of the chicken oviduct and the entire oviduct.
引用
收藏
页数:12
相关论文
共 50 条
  • [21] Validation of reference genes for the normalization of RT-qPCR gene expression in Acanthamoeba spp.
    Martina Köhsler
    David Leitsch
    Norbert Müller
    Julia Walochnik
    Scientific Reports, 10
  • [22] Identification of reference genes for RT-qPCR data normalization in Gammarus fossarum (Crustacea Amphipoda)
    Mehennaoui, Kahina
    Legay, Sylvain
    Serchi, Tommaso
    Guerold, Francois
    Giamberini, Laure
    Gutleb, Arno C.
    Cambier, Sebastien
    SCIENTIFIC REPORTS, 2018, 8
  • [23] Identification of Reference Genes for RT-qPCR Data Normalization in Cannabis sativa Stem Tissues
    Mangeot-Peter, Lauralie
    Legay, Sylvain
    Hausman, Jean-Francois
    Esposito, Sergio
    Guerriero, Gea
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (09):
  • [24] Selection of Reference Genes for Expression Normalization by RT-qPCR in Dracocephalum moldavica L.
    Li, Shasha
    Ge, Xiaomin
    Bai, Guoqing
    Chen, Chen
    CURRENT ISSUES IN MOLECULAR BIOLOGY, 2024, 46 (06) : 6284 - 6299
  • [25] RT-qPCR normalization of reference genes in different lifehistory stages of Gracilaria vermiculophylla(Rhodophyta)
    Yingyue ZHANG
    Jinxin YANG
    Ze YANG
    Cong QI
    Di XU
    Journal of Oceanology and Limnology, 2023, 41 (05) : 1910 - 1917
  • [26] Selection of reference genes suitable for normalization of RT-qPCR data in glioma stem cells
    Dang, Weiqi
    Zhang, Xiang
    Ma, Qinghua
    Chen, Lu
    Cao, Mianfu
    Miao, Jingya
    Cui, Youhong
    Zhang, Xia
    BIOTECHNIQUES, 2020, 68 (03) : 130 - 137
  • [27] Assessment of reference genes for reliable analysis of gene transcription by RT-qPCR in ovine leukocytes
    Mahakapuge, T. A. N.
    Scheerlinck, J-P Y.
    Rojas, C. A. Alvarez
    Every, A. L.
    Hagen, J.
    VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2016, 171 : 1 - 6
  • [28] Correction to: selection of reference genes for RT-qPCR analysis in developing chicken embryonic ovary
    Yi Wang
    Yu-Qing Zhang
    Zi-Wei Wu
    Ting Fang
    Fang Wang
    Han Zhao
    Zhi-Qiang Du
    Cai-Xia Yang
    Molecular Biology Reports, 2023, 50 : 10677 - 10677
  • [29] RT-qPCR Normalization Genes in the Red Alga Chondrus crispus
    Kowalczyk, Nathalie
    Rousvoal, Sylvie
    Herve, Cecile
    Boyen, Catherine
    Collen, Jonas
    PLOS ONE, 2014, 9 (02):
  • [30] Validation of reference genes for RT-qPCR normalization in common bean during biotic and abiotic stresses
    Aline Borges
    Siu Mui Tsai
    Danielle Gregorio Gomes Caldas
    Plant Cell Reports, 2012, 31 : 827 - 838