Primary structures of sperm-specific basic nuclear proteins and gene expression in Japanese newt, Cynops pyrrhogaster

• Published in: Molecular reproduction and development 1997-03, Vol.46 (3), p.243-251
• Main Authors: Yoshinobu, Kumiko, Kondo, Toshihiro, Takai, Masayuki, Katagiri, Chiaki, Tou, Hiroyuki, Abe, Shin-Ichi, Takamune, Kazufumi
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; amphibian; Animals; Base Sequence; Biological and medical sciences; Blotting, Northern; Cynops pyrrhogaster; DNA, Complementary - chemistry; Freshwater; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation, Developmental; In Situ Hybridization; Male; Molecular Sequence Data; Non mammalian vertebrate reproduction; Nuclear Proteins - chemistry; Nuclear Proteins - genetics; protamine; Protamines - genetics; RNA, Messenger - metabolism; Salamandridae; Sequence Alignment; spermatogenesis; testis; Vertebrates: reproduction; Xenopus Proteins
• ISSN: 1040-452X; 1098-2795
• DOI: 10.1002/(SICI)1098-2795(199703)46:3<243::AID-MRD2>3.0.CO;2-P

Electrophoretic analyses of acid extracts from mature sperm of newt, Cynops pyrrhogaster, on acid/urea/Triton X‐100 polyacrylamide gel showed the exclusive occurrence of sperm‐specific nuclear basic proteins (SBPs), which moved faster than somatic histones on the gel. These SBPs were eluted separately by reversed phase‐high‐performance liquid chromatography as two large peaks and a few small peaks. Of these, only the small peaks disappeared with treatment of the acid extracts with alkaline phosphatase before they were injected into the column, so that there were only two distinct components: NP1 and NP2. Determination of amino acid sequences by the Edman method as well as by sequencing of cDNA for both components indicated that each protein consisted of 43 (NP1) or 48 (NP2) amino acid residues, rich in arginine residues (53.5% in NP1; 47.9% in NP2), forming the clusters. They had molecular masses of 5,386 Da (NP1) and 5,748 Da (NP2), respectively. Northern blot analysis using cDNAs as probes indicated that mRNAs for both NP1 and NP2 occurred not in primary spermatocytes but in round spermatids. In situ hybridization analyses using antisense RNA for NP1 as a probe clearly showed the first appearance of NP1 mRNA at the late stage of round spermatid. Mol. Reprod. Dev. 46:243–251, 1997. © 1997 Wiley‐Liss, Inc.