The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Roles of DCL4 and DCL3b in rice phased small RNA biogenesis
Open accessAbstract
Summary: Higher plants have evolved multiple proteins in the RNase III family to produce and regulate different classes of small RNAs with specialized molecular functions. In rice (Oryza sativa), numerous genomic clusters are targeted by one of two microRNAs (miRNAs), miR2118 and miR2275, to produce secondary small interfering RNAs (siRNAs) of either 21 or 24 nucleotides in a phased manner. The biogenesis requirements or the functions of the phased small RNAs are completely unknown. Here we examine the rice Dicer‐Like (DCL) family, including OsDCL1, ‐3a, ‐3b and ‐4. By deep sequencing of small RNAs from different tissues of the wild type and osdcl4‐1, we revealed that the processing of 21‐nucleotide siRNAs, including trans‐acting siRNAs (tasiRNA) and over 1000 phased small RNA loci, was largely dependent on OsDCL4. Surprisingly, the processing of 24‐nucleotide phased small RNA requires the DCL3 homolog OsDCL3b rather than OsDCL3a, suggesting functional divergence within DCL3 family. RNA ligase‐mediated 5′ rapid amplification of cDNA ends and parallel analysis of RNA ends (PARE)/degradome analysis confirmed that most of the 21‐ and 24‐nucleotide phased small RNA clusters were initiated from the target sites of miR2118 and miR2275, respectively. Furthermore, the accumulation of the two triggering miRNAs requires OsDCL1 activity. Finally, we show that phased small RNAs are preferentially produced in the male reproductive organs and are likely to be conserved in monocots. Our results revealed significant roles of OsDCL4, OsDCL3b and OsDCL1 in the 21‐ and 24‐nucleotide phased small RNA biogenesis pathway in rice.
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Mfold web server for nucleic acid folding and hybridization prediction
Zuker, M. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg595 · Cited by 13,404
A germline-specific class of small RNAs binds mammalian Piwi proteins
Girard, A., Sachidanandam, R., Hannon, G. J., & Carmell, M. A. (2006) · Nature · doi:10.1038/nature04917 · Cited by 1,762
Cited by
Noncoding RNA: from dark matter to bright star
Xue, Y., Chen, R., Qu, L., & Cao, X. (2020) · Science China Life Sciences · doi:10.1007/s11427-020-1676-5 · Cited by 38
Self-citationThe RNA degradome: a precious resource for deciphering RNA processing and regulation codes in plants
Ma, X., Yin, X., Tang, Z., Ito, H., Shao, C., Meng, Y., & Xie, T. (2020) · RNA Biology · doi:10.1080/15476286.2020.1757898 · Cited by 17
Metadata
- Authors
- Song, X., Li, P., Zhai, J., Zhou, M., Ma, L., Liu, B., Jeong, D., Nakano, M., Cao, S., Liu, C., Chu, C., Wang, X., Green, P. J., Meyers, B. C., & Cao, X.
- Venue
- The Plant Journal
- Publisher
- Wiley
- Published
- 2011-11-23
- Volume
- 69
- Issue
- 3
- Pages
- 462-474
- ISSN
- 0960-7412 (ISSN-L)
- 1365-313X
- OpenAlex
- W1879776826
- Cited by
- 318
- References
- 2
- FWCI
- 21.43
- Type
- journal article
- Language
- en
- Open access
- bronze
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