Literature DB >> 16733265

Identification and expression analysis of Drosophila melanogaster genes encoding beta-hexosaminidases of the sperm plasma membrane.

F Cattaneo1, M E Pasini, J Intra, M Matsumoto, F Briani, M Hoshi, M E Perotti.   

Abstract

Sperm surface beta-N-acetylhexosaminidases are among the molecules mediating early gamete interactions in invertebrates and vertebrates, including man. The plasma membrane of Drosophila spermatozoa contains two beta-N-acetylhexosaminidases, DmHEXA and DmHEXB, which are required for egg fertilization. Here, we demonstrate that three putative Drosophila melanogaster genes predicted to code for beta-N-acetylhexosaminidases, Hexo1, Hexo2, and fdl, are all expressed in the male germ line. fdl codes for a homolog of the alpha-subunit of the mammalian lysosomal beta-N-acetylhexosaminidase Hex A. Hexo1 and Hexo2 encode two homologs of the beta-subunit of all known beta-N-acetylhexosaminidases, which we have named beta(1) and beta(2), respectively. Immunoblot analysis of sperm proteins indicated that the gene products associate in different heterodimeric combinations forming DmHEXA, with an alphabeta(2) structure, and DmHEXB, with a beta(1)beta(2) structure. Immunofluorescence demonstrated that all the gene products localized to the sperm plasma membrane. Although none of the genes was testis-specific, fdl was highly and preferentially expressed in the testis, whereas Hexo1 and Hexo2 showed broader tissue expression. Enzyme assays carried out on testis and on a variety of somatic tissues corroborated the results of gene expression analysis. These findings for the first time show the in vivo expression in insects of genes encoding beta-N-acetylhexosaminidases, the only molecules so far identified as involved in sperm/egg recognition in this class, whereas in mammals, the organisms where these enzymes have been best studied, only two types of polypeptide chains forming dimeric functional beta-N-acetylhexosaminidases are present in Drosophila three different gene products are available that might generate numerous dimeric isoforms.

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Year:  2006        PMID: 16733265     DOI: 10.1093/glycob/cwl007

Source DB:  PubMed          Journal:  Glycobiology        ISSN: 0959-6658            Impact factor:   4.313


  17 in total

1.  Β-hexosaminidase over-expression affects lysosomal glycohydrolases expression and glycosphingolipid metabolism in mammalian cells.

Authors:  Brunella Tancini; Alessandro Magini; Barbara Bortot; Alice Polchi; Lorena Urbanelli; Sandro Sonnino; Giovanni Maria Severini; Carla Emiliani
Journal:  Mol Cell Biochem       Date:  2011-12-07       Impact factor: 3.396

2.  Purification and characterization of a liver-derived beta-N-Acetylhexosaminidase from marine mammal Sotalia fluviatilis.

Authors:  J E Gomes Júnior; D S L Souza; R M Nascimento; A L M Lima; J A T Melo; T L Rocha; R N G Miller; O L Franco; M F Grossi-de-Sa; L R D Abreu
Journal:  Protein J       Date:  2010-04       Impact factor: 2.371

Review 3.  Let's talk about sexes: sex-related N-glycosylation in ecologically important invertebrates.

Authors:  Freja Scheys; Els J M Van Damme; Guy Smagghe
Journal:  Glycoconj J       Date:  2019-04-02       Impact factor: 2.916

4.  Structural determinants of an insect beta-N-Acetyl-D-hexosaminidase specialized as a chitinolytic enzyme.

Authors:  Tian Liu; Haitao Zhang; Fengyi Liu; Qingyue Wu; Xu Shen; Qing Yang
Journal:  J Biol Chem       Date:  2010-11-24       Impact factor: 5.157

5.  Release of Mediator Enzyme β-Hexosaminidase and Modulated Gene Expression Accompany Hemocyte Degranulation in Response to Parasitism in the Silkworm Bombyx mori.

Authors:  Shambhavi H Prabhuling; Pooja Makwana; Appukuttan Nair R Pradeep; Kunjupillai Vijayan; Rakesh Kumar Mishra
Journal:  Biochem Genet       Date:  2021-02-22       Impact factor: 1.890

6.  The expression profile and promoter analysis of β-N-acetylglucosaminidases in the silkworm Bombyx mori.

Authors:  Yuan-Fen Zhai; Ming-Xia Huang; Yu Wu; Guo-Dong Zhao; Jie Du; Bing Li; Wei-de Shen; Zheng-Guo Wei
Journal:  Mol Biol Rep       Date:  2014-07-08       Impact factor: 2.316

7.  Inactivation kinetics of formaldehyde on N-acetyl-β-D-glucosaminidase from Nile tilapia (Oreochromis niloticus).

Authors:  Wei-Ni Zhang; Ding-Ping Bai; Xin-Yu Lin; Qing-Xi Chen; Xiao-Hong Huang; Yi-Fan Huang
Journal:  Fish Physiol Biochem       Date:  2013-09-15       Impact factor: 2.794

8.  Molecular and biochemical characterization of a novel β-N-acetyl-D-hexosaminidase with broad substrate-spectrum from the Aisan corn borer, Ostrinia furnacalis.

Authors:  Fengyi Liu; Tian Liu; Mingbo Qu; Qing Yang
Journal:  Int J Biol Sci       Date:  2012-08-31       Impact factor: 6.580

9.  Drosophila spermiogenesis: Big things come from little packages.

Authors:  Lacramioara Fabian; Julie A Brill
Journal:  Spermatogenesis       Date:  2012-07-01

10.  Phylogenetic analyses suggest multiple changes of substrate specificity within the glycosyl hydrolase 20 family.

Authors:  Jari Intra; Giulio Pavesi; David S Horner
Journal:  BMC Evol Biol       Date:  2008-07-22       Impact factor: 3.260

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