Mutant generation of the testis genes and phenotype analyses in Drosophila
Received date: 2018-03-02
Revised date: 2018-04-27
Online published: 2018-05-11
Supported by
Supported by the Start-up Foundation from Nanjing Medical University(2012RC04);[Funding of State Key Laboratory of Reproductive Medicine(2012RC04)
Multiple genes work together to maintain the normal functions of the reproductive system. However, for many of these genes, little is known about their specific functions and mechanisms. In the present study, eight Drosophila genes, including CG4161, CG11475, CG2921, CG10541, CG7276, CG3800, CG8117 and CG16779, were selected for detailed studies based on their testis expression, undefined functions, and having highly homologous and conserved genes in humans (Homo sapiens) and mouse (Mus musculus). We analyzed their expression levels in different tissues, and determined their probably functions in male reproduction. The results showed that the first five genes were mainly expressed in testis, while other three showed ubiquitous expression in all tissues examined. Using the CRISPR/Cas9 (clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9) and homology-directed repair (HDR) strategies, we have systematically generated the mutants of these genes and studied their functions in male reproduction. Loss of function of CG7276 and CG3800 resulted in partial sterility and reduction of the offspring number, while other genes showed no significant impact on fertility. CG7276 -/- and CG3800 -/- mutants were partial sterile and showed various types of abnormities, including seminal vesicle atrophy, spermatogonial stem cell reduction and cellular distribution disorders. Results of DNA and F-actin staining also indicated that CG7276 and CG3800 could play important roles in spermiogenesis. The establishments of these mutants have provided means to unravel the functions and mechanisms of these genes in animal models.
Key words: testis; CRISPR/Cas9; drosophila; gene knockout
Junbo Tang, Haowei Cao, Rui Xu, Dandan Zhang, Juan Huang . Mutant generation of the testis genes and phenotype analyses in Drosophila[J]. Hereditas(Beijing), 2018 , 40(6) : 478 -487 . DOI: 10.16288/j.yczz.18-055
| [1] | Ikeda M, Chiba S, Ohashi K, Mizuno K . Furry protein promotes aurora a-mediated polo-like kinase 1 activation. J Biol Chem, 2012,287(33):27670-27681. | |||
| [2] | Baker CC, Fuller MT . Translational control of meiotic cell cycle progression and spermatid differentiation in male germ cells by a novel eIF4G homolog. Development, 2007,134(15):2863-2869. | |||
| [3] | Koerich LB, Wang XY, Clark AG, Carvalho AB . Low conservation of gene content in the Drosophila γ chromosome. Nature, 2008,456(7224):949-951. | |||
| [4] | Iyengar B, Luo NG, Farr CL, Kaguni LS, Campos AR . The accessory subunit of DNA polymerase γ is essential for mitochondrial DNA maintenance and development in Drosophila melanogaster. Proc Natl Acad Sci USA, 2002,99(7):4483-4488. | |||
| [5] | Goyal G, Fell B, Sarin A, Youle RJ, Sriram V . Role of mitochondrial remodeling in programmed cell death in Drosophila melanogaster. Dev Cell, 2007,12(5):807-816. | |||
| [6] | Hannigan MM, Zagore LL, Licatalosi DD . Ptbp2 controls an alternative splicing network required for cell communication during spermatogenesis. Cell Rep, 2017,19(12):2598-2612. | |||
| [7] | Zagore LL, Grabinski SE, Sweet TJ, Hannigan MM, Sramkoski RM, Li Q, Licatalosi DD . RNA binding protein Ptbp2 is essential for male germ cell development. Mol Cell Biol, 2015,35(23):4030-4042. | |||
| [8] | Sharma S, Hanukoglu A, Hanukoglu I . Localization of epithelial sodium channel (ENaC) and CFTR in the germinal epithelium of the testis, Sertoli cells, and spermatozoa. J Mol Histol, 2018,49(2):195-208. | |||
| [9] | Bhasin S, Mallidis C, Ma K . The genetic basis of infertility in men. Baillieres Best Pract Res Clin Endocrinol Metab, 2000,14(3):363-388. | |||
| [10] | Xu EY, Lee DF, Klebes A, Turek PJ, Kornberg TB, Pera RRAR . Human BOULE gene rescues meiotic defects in infertile flies. Hum Mol Genet, 2003,12(2):169-175. | |||
| [11] | Wu H, Sun LW, Wen Y, Liu YJ, Yu J, Mao FY, Wang Y, Tong C, Guo XJ, Hu ZB, Sha JH, Liu MX, Xia LX . Major spliceosome defects cause male infertility and are associated with nonobstructive azoospermia in humans. Proc Natl Acad Sci USA, 2016,113(15):4134-4139. | |||
| [12] | Siddall NA, Hime GR . A drosophila toolkit for defining gene function in spermatogenesis. Reproduction, 2017,153(4):R121-R132. | |||
| [13] | Xu J, Ren XJ, Sun J, Wang X, Qiao HH, Xu BW, Liu LP, Nie JQ . A toolkit of CRISPR-based genome editing systems in Drosophila. J Genet Genomic, 2015,42(4):141-149. | |||
| [14] | Port F, Chen HM, Lee T, Bullock SL . Optimized CRISPR/Cas tools for efficient germline and somatic genome engineering in Drosophila. Proc Natl Acad Sci USA, 2014,111(29):E2967
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