Previously Uncharacterized Histone Acetyltransferases Implicated in Mammalian Spermatogenesis

• Published in: Proceedings of the National Academy of Sciences - PNAS 2002-06, Vol.99 (13), p.8707-8712
• Main Authors: Lahn, Bruce T., Tang, Zhao Lan, Zhou, Jianxin, Barndt, Robert J., Parvinen, Martti, Allis, C. David, Page, David C.
• Format: Article
• Language: English
• Subjects: Acetylation; Acetyltransferases - metabolism; Acetyltransferases - physiology; Amino Acid Sequence; Animals; Base Sequence; Biological Sciences; Cellular biology; DNA Primers; Enzymes; Germ cells; Histone Acetyltransferases; Histones; Histones - metabolism; Humans; Immunohistochemistry; Infertility; Male; Males; Messenger RNA; Mice; Molecular Sequence Data; Nuclear Proteins; Proteins; Proteins - genetics; Proteins - metabolism; Recombinant proteins; Reverse Transcriptase Polymerase Chain Reaction; Saccharomyces cerevisiae Proteins; Sequence Homology, Amino Acid; Spermatids; Spermatids - metabolism; Spermatogenesis; Spermatogenesis - physiology; Spermiogenesis; Testes
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.082248899

During spermiogenesis (the maturation of spermatids into spermatozoa) in many vertebrate species, protamines replace histones to become the primary DNA-packaging protein. It has long been thought that this process is facilitated by the hyperacetylation of histone H4. However, the responsible histone acetyltransferase enzymes are yet to be identified. CDY is a human Y-chromosomal gene family expressed exclusively in the testis and implicated in male infertility. Its mouse homolog Cdyl, which is autosomal, is expressed abundantly in the testis. Proteins encoded by CDY and its homologs bear the "chromodomain," a motif implicated in chromatin binding. Here, we show that (i) human CDY and mouse CDYL proteins exhibit histone acetyltransferase activity in vitro, with a strong preference for histone H4; (ii) expression of human CDY and mouse Cdyl genes during spermatogenesis correlates with the occurrence of H4 hyperacetylation; and (iii) CDY and CDYL proteins are localized to the nuclei of maturing spermatids where H4 hyperacetylation takes place. Taken together, these data link human CDY and mouse CDYL to the histone-to-protamine transition in mammalian spermiogenesis. This link offers a plausible mechanism to account for spermatogenic failure in patients bearing deletions of the CDY genes.