PUBLICATION

Retrotransposons Mimic Germ Plasm Determinants to Promote Transgenerational Inheritance

Authors
Tiwari, B., Kurtz, P., Jones, A.E., Wylie, A., Amatruda, J.F., Boggupalli, D.P., Gonsalvez, G.B., Abrams, J.M.
ID
ZDB-PUB-171003-6
Date
2017
Source
Current biology : CB   27(19): 3010-3016.e3 (Journal)
Registered Authors
Amatruda, James F.
Keywords
Staufen, germ plasm, germline, mobile elements, molecular mimicry, oocyte, oskar, p53, transgenerational inheritance, transposons
MeSH Terms
  • Animals
  • Drosophila melanogaster/genetics*
  • Heredity/genetics
  • Oocytes/growth & development
  • Oocytes/metabolism*
  • RNA, Messenger/metabolism
  • Retroelements/genetics*
  • Zebrafish/genetics*
PubMed
28966088 Full text @ Curr. Biol.
Abstract
Retrotransposons are a pervasive class of mobile elements present in the genomes of virtually all forms of life [1, 2]. In metazoans, these are preferentially active in the germline, which, in turn, mounts defenses that restrain their activity [3, 4]. Here we report that certain classes of retrotransposons ensure transgenerational inheritance by invading presumptive germ cells before they are formed. Using sensitized Drosophila and zebrafish models, we found that diverse classes of retrotransposons migrate to the germ plasm, a specialized region of the oocyte that prefigures germ cells and specifies the germline of descendants in the fertilized egg. In Drosophila, we found evidence for a "stowaway" model, whereby Tahre retroelements traffic to the germ plasm by mimicking oskar RNAs and engaging the Staufen-dependent active transport machinery. Consistent with this, germ plasm determinants attracted retroelement RNAs even when these components were ectopically positioned in bipolar oocytes. Likewise, vertebrate retrotransposons similarly migrated to the germ plasm in zebrafish oocytes. Together, these results suggest that germ plasm targeting represents a fitness strategy adopted by some retrotransposons to ensure transgenerational propagation.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping