» Articles » PMID: 27402862

Poly(ADP-Ribosyl)ation of HnRNP A1 Protein Controls Translational Repression in Drosophila

Overview
Journal Mol Cell Biol
Specialty Cell Biology
Date 2016 Jul 13
PMID 27402862
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Poly(ADP-ribosyl)ation of heterogeneous nuclear ribonucleoproteins (hnRNPs) regulates the posttranscriptional fate of RNA during development. Drosophila hnRNP A1, Hrp38, is required for germ line stem cell maintenance and oocyte localization. The mRNA targets regulated by Hrp38 are mostly unknown. We identified 428 Hrp38-associated gene transcripts in the fly ovary, including mRNA of the translational repressor Nanos. We found that Hrp38 binds to the 3' untranslated region (UTR) of Nanos mRNA, which contains a translation control element. We have demonstrated that translation of the luciferase reporter bearing the Nanos 3' UTR is enhanced by dsRNA-mediated Hrp38 knockdown as well as by mutating potential Hrp38-binding sites. Our data show that poly(ADP-ribosyl)ation inhibits Hrp38 binding to the Nanos 3' UTR, increasing the translation in vivo and in vitro hrp38 and Parg null mutants showed an increased ectopic Nanos translation early in the embryo. We conclude that Hrp38 represses Nanos translation, whereas its poly(ADP-ribosyl)ation relieves the repression effect, allowing restricted Nanos expression in the posterior germ plasm during oogenesis and early embryogenesis.

Citing Articles

Cell-Type-Dependent Role for nsP3 Macrodomain ADP-Ribose Binding and Hydrolase Activity during Chikungunya Virus Infection.

Kim T, Abraham R, Pieterse L, Yeh J, Griffin D Viruses. 2022; 14(12).

PMID: 36560748 PMC: 9787352. DOI: 10.3390/v14122744.


hnRNP A1 in RNA metabolism regulation and as a potential therapeutic target.

Feng J, Zhou J, Lin Y, Huang W Front Pharmacol. 2022; 13:986409.

PMID: 36339596 PMC: 9634572. DOI: 10.3389/fphar.2022.986409.


Poly(ADP-ribosyl)ating pathway regulates development from stem cell niche to longevity control.

Bordet G, Kotova E, Tulin A Life Sci Alliance. 2021; 5(3).

PMID: 34949666 PMC: 8739260. DOI: 10.26508/lsa.202101071.


Poly(ADP-ribose) polymerase 1 in genome-wide expression control in Drosophila.

Bordet G, Lodhi N, Guo D, Kossenkov A, Tulin A Sci Rep. 2020; 10(1):21151.

PMID: 33273587 PMC: 7712786. DOI: 10.1038/s41598-020-78116-5.


Quantifying post-transcriptional regulation in the development of Drosophila melanogaster.

Becker K, Bluhm A, Casas-Vila N, Dinges N, Dejung M, Sayols S Nat Commun. 2018; 9(1):4970.

PMID: 30478415 PMC: 6255845. DOI: 10.1038/s41467-018-07455-9.

References
1.
Jin P, Duan R, Qurashi A, Qin Y, Tian D, Rosser T . Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndrome. Neuron. 2007; 55(4):556-64. PMC: 1994817. DOI: 10.1016/j.neuron.2007.07.020. View

2.
Oh J, Steward R . Bicaudal-D is essential for egg chamber formation and cytoskeletal organization in drosophila oogenesis. Dev Biol. 2001; 232(1):91-104. DOI: 10.1006/dbio.2001.0170. View

3.
Hanai S, Kanai M, Ohashi S, Okamoto K, Yamada M, Takahashi H . Loss of poly(ADP-ribose) glycohydrolase causes progressive neurodegeneration in Drosophila melanogaster. Proc Natl Acad Sci U S A. 2003; 101(1):82-6. PMC: 314142. DOI: 10.1073/pnas.2237114100. View

4.
Mallik M, Lakhotia S . Improved activities of CREB binding protein, heterogeneous nuclear ribonucleoproteins and proteasome following downregulation of noncoding hsromega transcripts help suppress poly(Q) pathogenesis in fly models. Genetics. 2010; 184(4):927-45. PMC: 2865928. DOI: 10.1534/genetics.109.113696. View

5.
Guruharsha K, Rual J, Zhai B, Mintseris J, Vaidya P, Vaidya N . A protein complex network of Drosophila melanogaster. Cell. 2011; 147(3):690-703. PMC: 3319048. DOI: 10.1016/j.cell.2011.08.047. View