Structure and expression of the highly repetitive histone H1‐related sperm chromatin proteins from winter flounder

• Published in: European journal of biochemistry Vol. 262; no. 2; pp. 258 - 267
• Main Authors: Watson, Catherine E., Gauthier, Sherry Y., Davies, Peter L.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Science Ltd 01.06.1999
• Subjects: Amino Acid Sequence; amino‐acid‐sequence repeats; Animals; Base Sequence; cDNA cloning; Chromatin - chemistry; Chromatin - genetics; chromatin‐associated protein; Cloning, Molecular; Codon; DNA, Complementary; Fish Proteins; Flounder - genetics; Genetic Linkage; histone H1; histones; Histones - chemistry; Histones - genetics; Male; Marine; Molecular Sequence Data; Pseudopleuronectes americanus; RNA, Messenger - genetics; Sequence Homology, Amino Acid; spermatogenesis; Spermatozoa - metabolism
• ISSN: 0014-2956; 1432-1033
• DOI: 10.1046/j.1432-1327.1999.00342.x

In the late stages of spermatogenesis, winter flounder produce a family of high molecular mass (80–200 kDa) basic nuclear proteins (HMrBNPs) that combine with the normal complement of histones to produce condensed sperm chromatin with an increased nucleosomal repeat length. The HMrBNPs have a biased amino‐acid composition in which Arg, Ser, Lys and Pro are abundant because of their presence in many simple peptide repeats. The organization of these repeats was deduced by cDNA cloning. The predominant repeating units are related 26‐ and 30‐amino‐acid sequences that in turn are linked by 6‐amino‐acid spacers to form 58‐ and 62‐amino‐acid repeats. Subsets of these repeats are also present, such as a dispersed 20‐amino‐acid repeat and a tandem array of nine heptapeptides at the C‐terminus. The HMrBNPs appear to have evolved from an extreme H1 variant that has an N‐terminal tail of HMrBNP‐like sequence linked to an H1 globular region. Based on sequences of the most abundant HMrBNP cDNAs, and the lack of hybridization between HMrBNP mRNAs and a DNA probe for the H1 globular region, the latter domain appears to have been lost during expansion and amplification of the HMrBNP‐like repeats. Transcripts of the HMrBNP and H1 variant genes are present in testis RNAs only during the mid‐spermatid stage of spermatogenesis, at the same time that HMrBNPs in their highly phosphorylated form first appear in the nucleus. Judging by the lack of a lag between HMrBNP mRNA synthesis and translation, the mRNAs for these highly basic proteins are not stored for any length of time. Instead, the deposition of HMrBNPs onto DNA, which coincides with the major reorganization and silencing of the chromatin, may be controlled by dephosphorylation.