References
- Aravin, A. A., G. W. van der Heijden, J. Castaneda, V. V. Vagin, G. J. Hannon, and A. Bortvin. 2009. Cytoplasmic compartmentalization of the fetal piRNA pathway in mice. PLoS Genet. 5:e1000764. https://doi.org/10.1371/journal.pgen.1000764
- Bak, C. W., T. K. Yoon, and Y. Choi. 2011. Functions of PIWI proteins in spermatogenesis. Clin. Exp. Reprod. Med. 38:61-67. https://doi.org/10.5653/cerm.2011.38.2.61
- Bao, J., L. Wang, J. Lei, Y. Hu, Y. Liu, H. Shen, W. Yan, and C. Xu. 2012. STK31(TDRD8) is dynamically regulated throughout mouse spermatogenesis and interacts with MIWI protein. Histochem. Cell Biol. 137:377-389. https://doi.org/10.1007/s00418-011-0897-9
- Bortvin, A. 2013. PIWI-interacting RNAs (piRNAs) - a mouse testis perspective. Biochemistry (Mosc) 78:592-602. https://doi.org/10.1134/S0006297913060059
- Callebaut, I. and J. P. Mornon. 1997. The human EBNA-2 coactivator p100: multidomain organization and relationship to the staphylococcal nuclease fold and to the tudor protein involved in Drosophila melanogaster development. Biochem. J. 321:125-132. https://doi.org/10.1042/bj3210125
- Caudy, A. A., R. F. Ketting, S. M. Hammond, A. M. Denli, A. M. Bathoorn, B. B. Tops, J. M. Silva, M. M. Myers, G. J. Hannon, and R. H. Plasterk. 2003. A micrococcal nuclease homologue in RNAi effector complexes. Nature 425:411-414. https://doi.org/10.1038/nature01956
- Chen, C., J. Jin, D. A. James, M. A. Adams-Cioaba, J. G. Park, Y. Guo, E. Tenaglia, C. Xu, G. Gish, J. Min, and T. Pawson. 2009. Mouse Piwi interactome identifies binding mechanism of Tdrkh Tudor domain to arginine methylated Miwi. Proc. Natl. Acad. Sci. USA 106:20336-20341. https://doi.org/10.1073/pnas.0911640106
- Chuma, S., M. Hiyoshi, A. Yamamoto, M. Hosokawa, K. Takamune, and N. Nakatsuji. 2003. Mouse Tudor Repeat-1 (MTR-1) is a novel component of chromatoid bodies/nuages in male germ cells and forms a complex with snRNPs. Mech. Dev. 120:979-990. https://doi.org/10.1016/S0925-4773(03)00181-3
- Chuma, S., M. Hosokawa, K. Kitamura, S. Kasai, M. Fujioka, M. Hiyoshi, K. Takamune, T. Noce, and N. Nakatsuji. 2006. Tdrd1/Mtr-1, a tudor-related gene, is essential for male germ-cell differentiation and nuage/germinal granule formation in mice. Proc. Natl. Acad. Sci. USA 103:15894-15899. https://doi.org/10.1073/pnas.0601878103
- Gao, X., X. Zhao, Y. Zhu, J. He, J. Shao, C. Su, Y. Zhang, W. Zhang, J. Saarikettu, O. Silvennoinen, Z. Yao, and J. Yang. 2012. Tudor staphylococcal nuclease (Tudor-SN) participates in small ribonucleoprotein (snRNP) assembly via interacting with symmetrically dimethylated Sm proteins. J. Biol. Chem. 287:18130-18141. https://doi.org/10.1074/jbc.M111.311852
- Garcia-Lopez, J., D. Hourcade Jde, and J. Del Mazo. 2013. Reprogramming of microRNAs by adenosine-to-inosine editing and the selective elimination of edited microRNA precursors in mouse oocytes and preimplantation embryos. Nucl. Acids Res. 41:5483-5493. https://doi.org/10.1093/nar/gkt247
- Handler, D., D. Olivieri, M. Novatchkova, F. S. Gruber, K. Meixner, K. Mechtler, A. Stark, R. Sachidanandam, and J. Brennecke. 2011. A systematic analysis of Drosophila TUDOR domain-containing proteins identifies Vreteno and the Tdrd12 family as essential primary piRNA pathway factors. EMBO J. 30:3977-3993. https://doi.org/10.1038/emboj.2011.308
- Kallajoki, M., I. Virtanen, and J. Suominen. 1986. The fate of acrosomal staining during the acrosome reaction of human spermatozoa as revealed by a monoclonal antibody and PNA-lectin. Int. J. Androl. 9:181-194. https://doi.org/10.1111/j.1365-2605.1986.tb00881.x
- Kotaja, N. and P. Sassone-Corsi. 2007. The chromatoid body: a germ-cell-specific RNA-processing centre. Nat. Rev. Mol. Cell Biol. 8:85-90.
- Lachke, S. A., F. S. Alkuraya, S. C. Kneeland, T. Ohn, A. Aboukhalil, G. R. Howell, I. Saadi, R. Cavallesco, Y. Yue, A. C. Tsai, K. S. Nair, M. I. Cosma, R. S. Smith, E. Hodges, S. M. Alfadhli, A. Al-Hajeri, H. E. Shamseldin, A. Behbehani, G. J. Hannon, M. L. Bulyk, A. V. Drack, P. J. Anderson, S. W. John, and R. L. Maas. 2011. Mutations in the RNA granule component TDRD7 cause cataract and glaucoma. Science 331:1571-1576. https://doi.org/10.1126/science.1195970
- Leverson, J. D., P. J. Koskinen, F. C. Orrico, E. M. Rainio, K. J. Jalkanen, A. B. Dash, R. N. Eisenman, and S. A. Ness. 1998. Pim-1 kinase and p100 cooperate to enhance c-Myb activity. Mol. Cell 2:417-425. https://doi.org/10.1016/S1097-2765(00)80141-0
- Li, C. L., W. Z. Yang, Y. P. Chen, and H. S. Yuan. 2008. Structural and functional insights into human Tudor-SN, a key component linking RNA interference and editing. Nucl. Acids Res. 36:3579-3589. https://doi.org/10.1093/nar/gkn236
- Luteijn, M. J. and R. F. Ketting. 2013. PIWI-interacting RNAs: From generation to transgenerational epigenetics. Nat. Rev. Genet. 14:523-534.
- Matzuk, M. M. and D. J. Lamb. 2008. The biology of infertility: Research advances and clinical challenges. Nat. Med. 14:1197-1213. https://doi.org/10.1038/nm.f.1895
- Meikar, O., M. Da Ros, H. Korhonen, and N. Kotaja. 2011. Chromatoid body and small RNAs in male germ cells. Reproduction 142:195-209. https://doi.org/10.1530/REP-11-0057
- Pan, J., M. Goodheart, S. Chuma, N. Nakatsuji, D. C. Page, and P. J. Wang. 2005. RNF17, a component of the mammalian germ cell nuage, is essential for spermiogenesis. Development 132:4029-4039. https://doi.org/10.1242/dev.02003
- Pandey, R. R., Y. Tokuzawa, Z. Yang, E. Hayashi, T. Ichisaka, S. Kajita, Y. Asano, T. Kunieda, R. Sachidanandam, S. Chuma, S. Yamanaka, and R. S. Pillai. 2013. Tudor domain containing 12 (TDRD12) is essential for secondary PIWI interacting RNA biogenesis in mice. Proc. Natl. Acad. Sci. USA 110:16492-16497. https://doi.org/10.1073/pnas.1316316110
- Paukku, K., N. Kalkkinen, O. Silvennoinen, K. K. Kontula, and J. Y. Lehtonen. 2008. p100 increases AT1R expression through interaction with AT1R 3'-UTR. Nucl. Acids Res. 36:4474-4487. https://doi.org/10.1093/nar/gkn411
- Reuter, M., S. Chuma, T. Tanaka, T. Franz, A. Stark, and R. S. Pillai. 2009. Loss of the Mili-interacting Tudor domaincontaining protein-1 activates transposons and alters the Mili-associated small RNA profile. Nat. Struct. Mol. Biol. 16:639-646. https://doi.org/10.1038/nsmb.1615
- Reynolds, N., B. Collier, K. Maratou, V. Bingham, R. M. Speed, M. Taggart, C. A. Semple, N. K. Gray, and H. J. Cooke. 2005. Dazl binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cells. Hum. Mol. Genet. 14:3899-3909. https://doi.org/10.1093/hmg/ddi414
- Saxe, J. P., M. Chen, H. Zhao, and H. Lin. 2013. Tdrkh is essential for spermatogenesis and participates in primary piRNA biogenesis in the germline. EMBO J. 32:1869-1885. https://doi.org/10.1038/emboj.2013.121
- Shoji, M., T. Tanaka, M. Hosokawa, M. Reuter, A. Stark, Y. Kato, G. Kondoh, K. Okawa, T. Chujo, T. Suzuki, K. Hata, S. L. Martin, T. Noce, S. Kuramochi-Miyagawa, T. Nakano, H. Sasaki, R. S. Pillai, N. Nakatsuji, and S. Chuma. 2009. The TDRD9-MIWI2 complex is essential for piRNA-mediated retrotransposon silencing in the mouse male germline. Dev. Cell 17:775-787. https://doi.org/10.1016/j.devcel.2009.10.012
- Smith, J. M., J. Bowles, M. Wilson, R. D. Teasdale, and P. Koopman. 2004. Expression of the tudor-related gene Tdrd5 during development of the male germline in mice. Gene Expr. Patterns 4:701-705. https://doi.org/10.1016/j.modgep.2004.04.002
- Tanaka, T., M. Hosokawa, V. V. Vagin, M. Reuter, E. Hayashi, A. L. Mochizuki, K. Kitamura, H. Yamanaka, G. Kondoh, K. Okawa, S. Kuramochi-Miyagawa, T. Nakano, R. Sachidanandam, G. J. Hannon, R. S. Pillai, N. Nakatsuji, and S. Chuma. 2011. Tudor domain containing 7 (Tdrd7) is essential for dynamic ribonucleoprotein (RNP) remodeling of chromatoid bodies during spermatogenesis. Proc. Natl. Acad. Sci. USA 108:10579-10584. https://doi.org/10.1073/pnas.1015447108
- van der Heijden, G. W., J. Castaneda, and A. Bortvin. 2010. Bodies of evidence - compartmentalization of the piRNA pathway in mouse fetal prospermatogonia. Curr. Opin. Cell Biol. 22:752-757. https://doi.org/10.1016/j.ceb.2010.08.014
- Vasileva, A., D. Tiedau, A. Firooznia, T. Muller-Reichert, and R. Jessberger. 2009. Tdrd6 is required for spermiogenesis, chromatoid body architecture, and regulation of miRNA expression. Curr. Biol. 19:630-639. https://doi.org/10.1016/j.cub.2009.02.047
- Wang, P. J., J. R. McCarrey, F. Yang, and D. C. Page. 2001. An abundance of X-linked genes expressed in spermatogonia. Nat. Genet. 27:422-426. https://doi.org/10.1038/86927
- Yabuta, Y., H. Ohta, T. Abe, K. Kurimoto, S. Chuma, and M. Saitou. 2011. TDRD5 is required for retrotransposon silencing, chromatoid body assembly, and spermiogenesis in mice. J. Cell Biol. 192:781-795. https://doi.org/10.1083/jcb.201009043
- Yang, J., S. Aittomaki, M. Pesu, K. Carter, J. Saarinen, N. Kalkkinen, E. Kieff, and O. Silvennoinen. 2002. Identification of p100 as a coactivator for STAT6 that bridges STAT6 with RNA polymerase II. EMBO J. 21:4950-4958. https://doi.org/10.1093/emboj/cdf463
- Ying, M. and D. Chen. 2012. Tudor domain-containing proteins of Drosophila melanogaster. Dev. Growth Differ. 54:32-43. https://doi.org/10.1111/j.1440-169X.2011.01308.x
Cited by
- Tdrd12 Is Essential for Germ Cell Development and Maintenance in Zebrafish vol.18, pp.6, 2017, https://doi.org/10.3390/ijms18061127
- Biased Duplications and Loss of Members in Tdrd Family in Teleost Fish vol.328, pp.8, 2017, https://doi.org/10.1002/jez.b.22757
- Structure and function of eTudor domain containing TDRD proteins vol.54, pp.2, 2016, https://doi.org/10.1080/10409238.2019.1603199
- The Role of the PRMT5-SND1 Axis in Hepatocellular Carcinoma vol.5, pp.1, 2016, https://doi.org/10.3390/epigenomes5010002