Literature DB >> 16386726

The extracellular protein coat of the inner acrosomal membrane is involved in zona pellucida binding and penetration during fertilization: characterization of its most prominent polypeptide (IAM38).

Yang Yu1, Wei Xu, Young-Joo Yi, Peter Sutovsky, Richard Oko.   

Abstract

A consequence of the acrosome reaction is to expose the inner acrosomal membrane (IAM), which is a requirement for the sperm's ability to secondarily bind to and then penetrate the zona pellucida (ZP) of the mammalian oocyte. However, the proteins on the IAM responsible for binding and presumably penetrating the zona have not been identified. This issue can be resolved if direct information is made available on the composition of the IAM. For this purpose, we devised a methodology in order to obtain a sperm head fraction consisting solely of the IAM bound to the detergent-resistant perinuclear theca. On the exposed IAM surface of this fraction, we defined an electron dense protein layer that we termed the IAM extracellular coat (IAMC), which was visible on sonicated and acrosome-reacted sperm of several mammalian species. High salt extraction removed the IAMC coincident with the removal of a prominent 38 kDa polypeptide, which we termed IAM38. Antibodies raised against this polypeptide confirmed its presence in the IAMC of intact, sonicated and acrosome-reacted sperm. By immunoscreening of a bovine testicular cDNA library and sequencing the resulting clones, we identified IAM38 as the equivalent of porcine Sp38 [Mori, E., Kashiwabara, S., Baba, T., Inagaki, Y., Mori, T., 1995. Amino acid sequences of porcine Sp38 and proacrosin required for binding to the zona pellucida. Dev. Biol., 168, 575-583], an intra-acrosomal protein with ZP-binding ability, whose precise localization in sperm was unknown. The blockage of IVF at the level of the zona with anti-IAM38 antibodies and the retention of IAM38 after sperm passage through the zona support its involvement in secondary sperm-zona binding. This study provides a novel approach to obtain direct information on the peripheral and integral protein composition of the IAM for identifying other candidates for sperm-zona interactions.

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Year:  2005        PMID: 16386726     DOI: 10.1016/j.ydbio.2005.11.003

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  21 in total

1.  Proteomic analysis of bovine sperm YWHA binding partners identify proteins involved in signaling and metabolism.

Authors:  Pawan Puri; Kimberley Myers; Douglas Kline; Srinivasan Vijayaraghavan
Journal:  Biol Reprod       Date:  2008-08-27       Impact factor: 4.285

2.  The chaperonin containing TCP1 complex (CCT/TRiC) is involved in mediating sperm-oocyte interaction.

Authors:  Matthew D Dun; Nathan D Smith; Mark A Baker; Minjie Lin; R John Aitken; Brett Nixon
Journal:  J Biol Chem       Date:  2011-08-31       Impact factor: 5.157

3.  Abnormal fertility, acrosome formation, IFT20 expression and localization in conditional Gmap210 knockout mice.

Authors:  Zhenyu Wang; Yuqin Shi; Suheng Ma; Qian Huang; Yi Tian Yap; Lin Shi; Shiyang Zhang; Ting Zhou; Wei Li; Bo Hu; Ling Zhang; Stephen A Krawetz; Gregory J Pazour; Rex A Hess; Zhibing Zhang
Journal:  Am J Physiol Cell Physiol       Date:  2019-10-02       Impact factor: 4.249

Review 4.  The Acrosomal Matrix.

Authors:  James A Foster; George L Gerton
Journal:  Adv Anat Embryol Cell Biol       Date:  2016       Impact factor: 1.231

5.  Loss of zona pellucida binding proteins in the acrosomal matrix disrupts acrosome biogenesis and sperm morphogenesis.

Authors:  Yi-Nan Lin; Angshumoy Roy; Wei Yan; Kathleen H Burns; Martin M Matzuk
Journal:  Mol Cell Biol       Date:  2007-07-30       Impact factor: 4.272

Review 6.  MMP2 and acrosin are major proteinases associated with the inner acrosomal membrane and may cooperate in sperm penetration of the zona pellucida during fertilization.

Authors:  Marvin Ferrer; Hilma Rodriguez; Lindsay Zara; Yang Yu; Wei Xu; Richard Oko
Journal:  Cell Tissue Res       Date:  2012-05-22       Impact factor: 5.249

7.  Sperm proteasomes degrade sperm receptor on the egg zona pellucida during mammalian fertilization.

Authors:  Shawn W Zimmerman; Gaurishankar Manandhar; Young-Joo Yi; Satish K Gupta; Miriam Sutovsky; John F Odhiambo; Michael D Powell; David J Miller; Peter Sutovsky
Journal:  PLoS One       Date:  2011-02-23       Impact factor: 3.240

8.  The testicular and epididymal expression profile of PLCζ in mouse and human does not support its role as a sperm-borne oocyte activating factor.

Authors:  Mahmoud Aarabi; Yang Yu; Wei Xu; Man Y Tse; Stephen C Pang; Young-Joo Yi; Peter Sutovsky; Richard Oko
Journal:  PLoS One       Date:  2012-03-12       Impact factor: 3.240

9.  The sensitivity of murine spermiogenesis to miglustat is a quantitative trait: a pharmacogenetic study.

Authors:  Wilhelm Bone; Charlotte M Walden; Martin Fritsch; Ulrike Voigtmann; Eckhard Leifke; Ulrich Gottwald; Stephanie Boomkamp; Frances M Platt; Aarnoud C van der Spoel
Journal:  Reprod Biol Endocrinol       Date:  2007-01-22       Impact factor: 5.211

10.  Evolution of genes involved in gamete interaction: evidence for positive selection, duplications and losses in vertebrates.

Authors:  Camille Meslin; Sylvie Mugnier; Isabelle Callebaut; Michel Laurin; Géraldine Pascal; Anne Poupon; Ghylène Goudet; Philippe Monget
Journal:  PLoS One       Date:  2012-09-05       Impact factor: 3.240

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