TNP1
Spermatid nuclear transition protein 1 is a protein that in humans is encoded by the TNP1 gene.[1][2]
References
Further reading
- Meistrich ML, Mohapatra B, Shirley CR, Zhao M (2004). "Roles of transition nuclear proteins in spermiogenesis.". Chromosoma 111 (8): 483–8. doi:10.1007/s00412-002-0227-z. PMID 12743712.
- Chirat F, Martinage A, Briand G et al. (1991). "Nuclear transition protein 1 from ram elongating spermatids. Mass spectrometric characterization, primary structure and phosphorylation sites of two variants.". Eur. J. Biochem. 198 (1): 13–20. doi:10.1111/j.1432-1033.1991.tb15980.x. PMID 2040274.
- Baskaran R, Rao MR (1991). "Interaction of spermatid-specific protein TP2 with nucleic acids, in vitro. A comparative study with TP1.". J. Biol. Chem. 265 (34): 21039–47. PMID 2250010.
- Kleene KC, Borzorgzadeh A, Flynn JF et al. (1988). "Nucleotide sequence of a cDNA clone encoding mouse transition protein 1.". Biochim. Biophys. Acta 950 (2): 215–20. doi:10.1016/0167-4781(88)90013-9. PMID 3382664.
- Luerssen H, Hoyer-Fender S, Engel W (1988). "The nucleotide sequence of human transition protein 1 cDNA.". Nucleic Acids Res. 16 (15): 7723. doi:10.1093/nar/16.15.7723. PMC 338445. PMID 3412903.
- Akama K, Kojima S, Nakano M et al. (1994). "The amino acid sequence and phosphorylation sites of a boar transition protein 1.". Biochem. Mol. Biol. Int. 32 (2): 349–57. PMID 8019440.
- Steger K, Klonisch T, Gavenis K et al. (1999). "Expression of mRNA and protein of nucleoproteins during human spermiogenesis.". Mol. Hum. Reprod. 4 (10): 939–45. doi:10.1093/molehr/4.10.939. PMID 9809674.
- Yu YE, Zhang Y, Unni E et al. (2000). "Abnormal spermatogenesis and reduced fertility in transition nuclear protein 1-deficient mice.". Proc. Natl. Acad. Sci. U.S.A. 97 (9): 4683–8. doi:10.1073/pnas.97.9.4683. PMC 18293. PMID 10781074.
- Siffroi JP, Alfonsi MF, Dadoune JP (2001). "Electron microscopic in situ hybridization study of simultaneous expression of TNP1 and PRM1 genes in human spermatids.". Italian journal of anatomy and embryology = Archivio italiano di anatomia ed embriologia 103 (4 Suppl 1): 65–74. PMID 11315969.
- Strausberg RL, Feingold EA, Grouse LH et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Gerhard DS, Wagner L, Feingold EA et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Miyagawa Y, Nishimura H, Tsujimura A et al. (2006). "Single-nucleotide polymorphisms and mutation analyses of the TNP1 and TNP2 genes of fertile and infertile human male populations.". J. Androl. 26 (6): 779–86. doi:10.2164/jandrol.05069. PMID 16291974.
- Jedrzejczak P, Kempisty B, Bryja A et al. (2007). "Quantitative assessment of transition proteins 1, 2 spermatid-specific linker histone H1-like protein transcripts in spermatozoa from normozoospermic and asthenozoospermic men.". Arch. Androl. 53 (4): 199–205. doi:10.1080/01485010701426430. PMID 17852044.
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| Envelope (membrane)/
nuclear lamina | |
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| | Nucleolus | |
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| | Other | |
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| see also nucleus diseases
Index of cells |
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| | Description |
- Structure
- Organelles
- peroxisome
- cytoskeleton
- centrosome
- epithelia
- cilia
- mitochondria
- Membranes
- Membrane transport
- ion channels
- vesicular transport
- solute carrier
- ABC transporters
- ATPase
- oxidoreduction-driven
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| | Disease |
- Structural
- peroxisome
- cytoskeleton
- cilia
- mitochondria
- nucleus
- scleroprotein
- Membrane
- channelopathy
- solute carrier
- ATPase
- ABC transporters
- other
- extracellular ligands
- cell surface receptors
- intracellular signalling
- Vesicular transport
- Pore-forming toxins
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