» Articles » PMID: 17409063

The Centromeric Retrotransposons of Rice Are Transcribed and Differentially Processed by RNA Interference

Overview
Journal Genetics
Specialty Genetics
Date 2007 Apr 6
PMID 17409063
Citations 32
Authors
Affiliations
Soon will be listed here.
Abstract

Retrotransposons consist of significant portions of many complex eukaryotic genomes and are often enriched in heterochromatin. The centromeric retrotransposon (CR) family in grass species is colonized in the centromeres and highly conserved among species that have been diverged for >50 MY. These unique characteristics have inspired scientists to speculate about the roles of CR elements in organization and function of centromeric chromatin. Here we report that the CRR (CR of rice) elements in rice are highly enriched in chromatin associated with H3K9me2, a hallmark for heterochromatin. CRR elements were transcribed in root, leaf, and panicle tissues, suggesting a constitutive transcription of this retrotransposon family. However, the overall transcription level was low and the CRR transcripts appeared to be derived from relatively few loci. The majority of the CRR transcripts had chimerical structures and contained only partial CRR sequences. We detected small RNAs (smRNAs) cognate to nonautonomous CRR1 (noaCRR1) and CRR1, but not CRR2 elements. This result was also confirmed by in silico analysis of rice smRNA sequences. These results suggest that different CRR subfamilies may play different roles in the RNAi-mediated pathway for formation and maintenance of centromeric heterochromatin.

Citing Articles

Evolution of Einkorn wheat centromeres is driven by the mutualistic interplay of two LTR retrotransposons.

Heuberger M, Koo D, Ahmed H, Tiwari V, Abrouk M, Poland J Mob DNA. 2024; 15(1):16.

PMID: 39103880 PMC: 11302176. DOI: 10.1186/s13100-024-00326-9.


Transposable elements: multifunctional players in the plant genome.

Hassan A, Mokhtar M, El Allali A Front Plant Sci. 2024; 14:1330127.

PMID: 38239225 PMC: 10794571. DOI: 10.3389/fpls.2023.1330127.


Centromeric and pericentric transcription and transcripts: their intricate relationships, regulation, and functions.

Zhu J, Guo Q, Choi M, Liang Z, Yuen K Chromosoma. 2023; 132(3):211-230.

PMID: 37401943 PMC: 10356649. DOI: 10.1007/s00412-023-00801-x.


Retrotransposons: How the continuous evolutionary front shapes plant genomes for response to heat stress.

Papolu P, Ramakrishnan M, Mullasseri S, Kalendar R, Wei Q, Zou L Front Plant Sci. 2022; 13:1064847.

PMID: 36570931 PMC: 9780303. DOI: 10.3389/fpls.2022.1064847.


Differential nuclease sensitivity profiling uncovers a drought responsive change in maize leaf chromatin structure for two large retrotransposon derivatives, and .

Park M, Williams D, Turpin Z, Wiggins Z, Tsolova V, Onokpise O Plant Direct. 2021; 5(8):e337.

PMID: 34430792 PMC: 8365550. DOI: 10.1002/pld3.337.


References
1.
Brodie R, Roper R, Upton C . JDotter: a Java interface to multiple dotplots generated by dotter. Bioinformatics. 2004; 20(2):279-81. DOI: 10.1093/bioinformatics/btg406. View

2.
Li Z, Chen S, Zheng X, Zhu L . Identification and chromosomal localization of a transcriptionally active retrotransposon of Ty3-gypsy type in rice. Genome. 2000; 43(2):404-8. DOI: 10.1139/g99-137. View

3.
Bernstein E, Allis C . RNA meets chromatin. Genes Dev. 2005; 19(14):1635-55. DOI: 10.1101/gad.1324305. View

4.
Gorinsek B, Gubensek F, Kordis D . Evolutionary genomics of chromoviruses in eukaryotes. Mol Biol Evol. 2004; 21(5):781-98. DOI: 10.1093/molbev/msh057. View

5.
Wilhelm M, Wilhelm F . Reverse transcription of retroviruses and LTR retrotransposons. Cell Mol Life Sci. 2001; 58(9):1246-62. PMC: 11337404. DOI: 10.1007/PL00000937. View