Chen H, Lin GW, Liu ZK, Chen W, Xie YQ, Wang XC (2010) Study on growth characters of cultured Pseudosciaena crocea originated from eastern fujian. Marine Sciences. 34: 1-5. https://doi.org/10.3724/SP.J.1238.2010.00453
Chu PJ, Rivera JF, Arnold DB (2006) A role for KIF17 in transport of Kv4.2. J. Biol. Chem. 281: 365–373. https://doi.org/10.1074/jbc.M508897200
Goodson HV, Jonasson EM (2018) Microtubules and Microtubule-Associated Proteins. Cold Spring Harbor Perspect. Biol. 10. https://doi.org/10.1101/cshperspect.a022608
Hammond JW, Blasius TL, Soppina V, Cai D, Verhey KJ (2010) Autoinhibition of the kinesin-2 motor KIF17 via dual intramolecular mechanisms. J. Cell Biol. 189: 1013–1025. https://doi.org/10.1083/jcb.201001057
Hermo L, Pelletier RM, Cyr DG, Smith CE (2010a) Surfing the wave, cycle, life history, and genes/proteins expressed by testicular germ cells. Part 2: changes in spermatid organelles associated with development of spermatozoa. Microsc. Res. Tech. 73: 279–319. https://doi.org/10.1002/jemt.20787
Hirokawa N, Takemura R (2005) Molecular motors and mechanisms of directional transport in neurons. Nat. Rev. Neurosci. 6: 201-214. https://doi.org/10.2169/internalmedicine.37.65
Hogeveen KN, Sassone-Corsi P (2006) Regulation of gene expression in post-meiotic male germ cells: CREM-signalling pathways and male fertility. Hum. Fertil. 9: 73-79. https://doi.org/10.1080/14647270500463400
Kayadjanian N, Lee HS, Pina-Crespo J, Heinemann SF (2007) Localization of glutamate receptors to distal dendrites depends on subunit composition and the kinesin motor protein KIF17. Mol. Cell. Neurosci. 34: 219–230. https://doi.org/10.1016/j.mcn.2006.11.001
Kierszenbaum AL (2002) Intramanchette transport (IMT): managing the making of the spermatid head, centrosome and tail. Mol. Reprod. Dev. 63: 1–4. https://doi.org/10.1002/mrd.10179
Kierszenbaum AL, Tres LL (2004) The acrosome-acroplaxome-manchette complex and the shaping of the spermatid head. Arch. Histol. Cytol. 67: 271–284. https://doi.org/10.1679/aohc.67.271
Kimmins S, Kotaja N, Fienga G, Kolthur US, Brancorsini S, Hogeveen K, Monaco L, Sassone-Corsi P (2004) A specific programme of gene transcription in male germ cells. Reprod. BioMed. Online. 8: 496-500. https://doi.org/10.1016/S1472-6483(10)61094-2
Lawrence CJ, Dawe RK, Christie KR, Cleveland DW, Dawson SC, Endow SA, Goldstein LSB, Goodson HV, Hirokawa N, Howard J, Malmberg RL, McIntosh JR, Miki H, Mitchison TJ, Okada Y, Reddy ASN, Saxton WM, Schliwa M, Scholey JM, Vale RD, Walzak CE, Wordeman LA (2004) A standardized kinesin nomenclature. J. Cell. Biol. 167: 19-22. https://doi.org/10.1083/jcb.200408113
Lehti MS, Kotaja N, Sironen A (2013) KIF3A is essential for sperm tail formation and manchette function. Mol. Cell. Endocrinol. 377: 44-55. https://doi.org/10.1016/j.mce.2013.06.030
Liang YJ, Ni JH, Wang LM, Tan FQ, Yang WX (2020) KIF3A regulates the Wnt/β-catenin pathway via transporting β-catenin during spermatogenesis in Eriocheir sinensis. Cell Tissue Res. 381. https://doi.org/10.1007/s00441-020-03220-x
Luo SY, Gao XM, Ding J, Liu C, Du C, Hou CC, Zhu JQ, Lou B (2019) Transcriptome sequencing reveals the traits of spermatogenesis and testicular development in large yellow croaker (Larimichthys crocea). Genes. 10. https://doi.org/10.3390/genes10120958
Ma DD, Wang DH, Yang WX (2017) Kinesins in spermatogenesis. Biol. Reprod. 96: 267-276. https://doi.org/10.1095/biolreprod.116.144113
Macho B (2002) CREM-Dependent transcription in male germ cells controlled by a kinesin. Science. 298: 2388-2390. https://doi.org/10.1126/science.1077265
Meistrich ML (1993) Nuclear Morphogenesis during Spermiogenesis-ScienceDirect. Molecular Biology of the Male Reproductive System. https://doi.org/10.1016/B978-0-08-091764-1.50007-6
Meistrich ML, Trostle-Weige PK, Russell LD (1990) Abnormal manchette development in spermatids of azh/azh mutant mice. Am. J. Anat. 188: 74–86. https://doi.org/10.1002/aja.1001880109
Miki H, Okada Y, Hirokawa N (2005) Analysis of the kinesin superfamily: insights into structure and function. Trends Cell Biol. 15: 467-476. https://doi.org/10.1016/j.tcb.2005.07.006
Mochida K, Tres LL, Kierszenbaum AL (1998) Isolation of the rat spermatid manchette and its perinuclear ring. Dev. Biol. 200: 46–56. https://doi.org/10.1006/dbio.1998.8942
Mu Dl, Du C, Fu SY, Wang JQ, Hou CC, Tang DJ, Zhu JQ (2019) Molecular Characterization, Tissue Distribution and Localization of Larimichthys crocea Kif3a and Kif3b and Expression Analysis of Their Genes During Spermiogenesis. J. Ocean Univ. China. 18: 1451–1469. https://doi.org/10.1007/s11802-019-3987-2
Navolanic PM, Sperry AO (2000) Identification of isoforms of a mitoticmotor in mammalian spermatogenesis. Biol. Reprod. 62: 1360–1369. https://doi.org/10.1095/biolreprod62.5.1360
O’Donnell L, O’Bryan MK (2014) Microtubules and spermatogenesis. Semin. Cell Dev. Biol. 30: 45–54. https://doi.org/10.1016/j.semcdb.2014.01.003
Rivkin E, Cullinan E, Tres L, Kierszenbaum A (1997) A protein associated with the manchette during rat spermiogenesis is encoded by a gene of the TBP-1-like subfamily with highly conserved ATPase and protease domains. Mol. Reprod. Dev. 48: 77–89. https://doi.org/10.1002/(SICI)1098-2795(199709)48:1<77::AID-MRD10>3.0.CO;2-T
Saade M, Irla M, Govin J, Victorero G, Samson M, Nguyen C (2007) Dynamic distribution of spatial during mouse spermatogenesis and its interaction with the kinesin KIF17b. Exp. Cell Res. 313: 614-626. https://doi.org/10.1016/j.yexcr.2006.11.011
Setou M (2000) Kinesin Superfamily Motor Protein KIF17 and mLin-10 in NMDA Receptor-Containing Vesicle Transport. Science. 288: 1796-802. https://doi.org/10.1126/science.288.5472.1796
Silverman MA, Leroux MR (2009) Intraflagellar transport and the generation of dynamic, structurally and functionally diverse cilia. Trends Cell Biol. 19: 306-316. https://doi.org/10.1016/j.tcb.2009.04.002
Soley J (1997) Nuclear morphogenesis and the role of the manchette during spermiogenesis in the ostrich (Struthio camelus). J. Anat. 190: 563–576. https://doi.org/10.1046/j.1469-7580.1997.19040563.x
Tres L, Kierszenbaum A (1996) Sak57, an acidic keratin initially present in the spermatid manchette before becoming a component of paraaxonemal structures of the developing tail. Mol. Reprod. Dev. 44: 395–407. https://doi.org/10.1002/(SICI)1098-2795(199607)44:33.0.CO;2-#
Wang JQ, Gao XM, Zheng XB, Hou CC, Xie QP, Lou B, Zhu JQ (2019) Expression and potential functions of kif3a/3b to promote nuclear reshaping and tail formation during Larimichthys polyactis spermiogenesis. Dev. Genes Evol. 229: 161–181. https://doi.org/10.1007/s00427-019-00637-5
Zhang B, Xue D, Wang J, Li Y, Liu J (2016) Development and preliminary evaluation of a genomewide single nucleotide polymorphisms resource generated by rad‐seq for the small yellow croaker (Larimichthys polyactis). Mol Ecol Resour. 16: 755–768. https://doi.org/10.1111/1755-0998.12476
Zhang DD, Gao XM, Zhao YQ, Hou CC, Zhu JQ (2017) The C-terminal kinesin motor KIFC1 may participate in nuclear reshaping and flagellum formation during spermiogenesis of Larimichthys crocea. Fish Physiol. Biochem. 43: 1351–1371. https://doi.org/10.1007/s10695-017-0377-9