Epigenetic marking of sperm by post-translational modification of histones and protamines

被引:125
|
作者
Brunner, Andrea M. [1 ,4 ]
Nanni, Paolo [2 ,3 ]
Mansuy, Isabelle M. [1 ]
机构
[1] Univ Zurich, Fac Med, Brain Res Inst, Neurosci Ctr Zurich,ETH Zurich,Dept Hlth Sci & Te, CH-8057 Zurich, Switzerland
[2] Univ Zurich, Funct Genom Ctr Zurich, CH-8057 Zurich, Switzerland
[3] Swiss Fed Inst Technol, CH-8057 Zurich, Switzerland
[4] Univ Utrecht, NL-3584 CH Utrecht, Netherlands
关键词
Epigenetics; Mouse sperm; Histones; Protamines; Post-translational modifications; Mass spectrometry; Electron transfer dissociation; Intact protein analysis; Top down; Proteoforms; MASS-SPECTROMETRY; CHROMATIN; IDENTIFICATION; PHOSPHORYLATION; ACETYLATION; INHERITANCE; VARIANTS;
D O I
10.1186/1756-8935-7-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: The concept that individual traits can be acquired and transmitted by the germline through epigenetic mechanisms has gained recognition in the past years. However, epigenetic marks in sperm have not been are not well identified. Results: Using a novel proteomic approach that combines peptide-based bottom-up and intact protein top-down tandem mass spectrometry, we report the identification of epigenetic marks on histones and protamines in adult mouse sperm. We identified a total of 26 post-translational modifications (PTMs) on specific residues of the core histones H2B, H3 and H4, and the linker histone H1, four of which had not been described previously in any tissue or cell line. We also detected 11 novel PTMs on the protamines PRM1 and PRM2 and observed that they are present in specific combinations on individual protamines. Conclusions: Both histones and protamines carry multiple PTMs in the adult mouse sperm. On protamines, specific PTM combinations might form a 'protamine code' similar to the 'histone code'. These findings suggest a potential role for PTMs on sperm histones and protamines in epigenetic signatures underlying transgenerational inheritance.
引用
收藏
页数:12
相关论文
共 50 条
  • [41] Post-translational modification of RAS proteins
    Campbell, Sharon L.
    Philips, Mark R.
    CURRENT OPINION IN STRUCTURAL BIOLOGY, 2021, 71 : 180 - 192
  • [42] Progresses in Predicting Post-translational Modification
    Kuo-Chen Chou
    International Journal of Peptide Research and Therapeutics, 2020, 26 : 873 - 888
  • [44] Post-translational modification of the androgen receptor
    Gioeli, Daniel
    Paschal, Bryce M.
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2012, 352 (1-2) : 70 - 78
  • [45] Deciphering post-translational modification codes
    Lothrop, Adam P.
    Torres, Matthew P.
    Fuchs, Stephen M.
    FEBS LETTERS, 2013, 587 (08) : 1247 - 1257
  • [46] AMPylation is a new post-translational modiFICation
    Yarbrough, Melanie L.
    Orth, Kim
    NATURE CHEMICAL BIOLOGY, 2009, 5 (06) : 378 - 379
  • [48] Global Post-Translational Modification Discovery
    Li, Qiyao
    Shortreed, Michael R.
    Wenger, Craig D.
    Frey, Brian L.
    Schaffer, Leah V.
    Scalf, Mark
    Smith, Lloyd M.
    JOURNAL OF PROTEOME RESEARCH, 2017, 16 (04) : 1383 - 1390
  • [49] Functional analysis tools for post-translational modification: a post-translational modification database for analysis of proteins and metabolic pathways
    Cruz, Edward R.
    Nguyen, Hung
    Nguyen, Tin
    Wallace, Ian S.
    PLANT JOURNAL, 2019, 99 (05): : 1003 - 1013