» Articles » PMID: 23064230

Structure and Function of Zucchini Endoribonuclease in PiRNA Biogenesis

Overview
Journal Nature
Specialty Science
Date 2012 Oct 16
PMID 23064230
Citations 187
Authors
Affiliations
Soon will be listed here.
Abstract

PIWI-interacting RNAs (piRNAs) silence transposons to maintain genome integrity in animal germ lines. piRNAs are classified as primary and secondary piRNAs, depending on their biogenesis machinery. Primary piRNAs are processed from long non-coding RNA precursors transcribed from piRNA clusters in the genome through the primary processing pathway. Although the existence of a ribonuclease participating in this pathway has been predicted, its molecular identity remained unknown. Here we show that Zucchini (Zuc), a mitochondrial phospholipase D (PLD) superfamily member, is an endoribonuclease essential for primary piRNA biogenesis. We solved the crystal structure of Drosophila melanogaster Zuc (DmZuc) at 1.75 Å resolution. The structure revealed that DmZuc has a positively charged, narrow catalytic groove at the dimer interface, which could accommodate a single-stranded, but not a double-stranded, RNA. DmZuc and the mouse homologue MmZuc (also known as Pld6 and MitoPLD) showed endoribonuclease activity for single-stranded RNAs in vitro. The RNA cleavage products bear a 5'-monophosphate group, a hallmark of mature piRNAs. Mutational analyses revealed that the conserved active-site residues of DmZuc are critical for the ribonuclease activity in vitro, and for piRNA maturation and transposon silencing in vivo. We propose a model for piRNA biogenesis in animal germ lines, in which the Zuc endoribonuclease has a key role in primary piRNA maturation.

Citing Articles

Landscape of small nucleic acid therapeutics: moving from the bench to the clinic as next-generation medicines.

Liu M, Wang Y, Zhang Y, Hu D, Tang L, Zhou B Signal Transduct Target Ther. 2025; 10(1):73.

PMID: 40059188 PMC: 11891339. DOI: 10.1038/s41392-024-02112-8.


A guide to the biogenesis and functions of endogenous small non-coding RNAs in animals.

Jouravleva K, Zamore P Nat Rev Mol Cell Biol. 2025; .

PMID: 39856370 DOI: 10.1038/s41580-024-00818-9.


piRNA Defense Against Endogenous Retroviruses.

Abajorga M, Yurkovetskiy L, Luban J Viruses. 2024; 16(11).

PMID: 39599869 PMC: 11599104. DOI: 10.3390/v16111756.


Advances in PIWI-piRNA function in female reproduction in mammals.

Lv X, Zhang H, Wu L Acta Biochim Biophys Sin (Shanghai). 2024; 57(1):148-156.

PMID: 39544003 PMC: 11802344. DOI: 10.3724/abbs.2024195.


Crystal structure of Alzheimer's disease phospholipase D3 provides a molecular basis for understanding its normal and pathological functions.

Ishii K, Hermans S, Georgopoulou M, Nero T, Hancock N, Crespi G FEBS J. 2024; 291(24):5398-5419.

PMID: 39325669 PMC: 11653685. DOI: 10.1111/febs.17277.


References
1.
Fukuhara S, Nishimasu H, Bonnefond L, Matsumoto N, Ishitani R, Nureki O . Expression, purification, crystallization and preliminary X-ray crystallographic analysis of Zucchini from Drosophila melanogaster. Acta Crystallogr Sect F Struct Biol Cryst Commun. 2012; 68(Pt 11):1346-50. PMC: 3515378. DOI: 10.1107/S1744309112038936. View

2.
Pillai R, Chuma S . piRNAs and their involvement in male germline development in mice. Dev Growth Differ. 2012; 54(1):78-92. DOI: 10.1111/j.1440-169X.2011.01320.x. View

3.
Leiros I, Secundo F, Zambonelli C, Servi S, Hough E . The first crystal structure of a phospholipase D. Structure. 2000; 8(6):655-67. DOI: 10.1016/s0969-2126(00)00150-7. View

4.
Huang H, Gao Q, Peng X, Choi S, Sarma K, Ren H . piRNA-associated germline nuage formation and spermatogenesis require MitoPLD profusogenic mitochondrial-surface lipid signaling. Dev Cell. 2011; 20(3):376-87. PMC: 3061402. DOI: 10.1016/j.devcel.2011.01.004. View

5.
Saito K, Nishida K, Mori T, Kawamura Y, Miyoshi K, Nagami T . Specific association of Piwi with rasiRNAs derived from retrotransposon and heterochromatic regions in the Drosophila genome. Genes Dev. 2006; 20(16):2214-22. PMC: 1553205. DOI: 10.1101/gad.1454806. View