Published in: Gene, vol. 377, 1 August 2006, Pages 186-194
doi:10.1016/j.gene.2006.04.010
http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T39-4JW0WRW-3&_coverDate=08%2F01%2F2006&_alid=426318946&_rdoc=1&_fmt=&_orig=search&_qd=1&_cdi=4941&_sort=d&view=c&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=2ef77ebd4c8d4beff3439ce012f0d011

"Accumulation of sense–antisense transcripts of the rice catalase gene CatB under dark conditions requires signals from shoots".

Masao Iwamoto  a, @, and Kenichi Higob b

a Plant Physiology Department, National Institute of Agrobiological Sciences, 2-1-2, Kannondai, Tsukuba, Ibaraki 305-8602, Japan
b Molecular Genetics Department, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602, Japan

@ Corresponding author. Tel./fax: +81 29 838 8384
E-mail: iwamas@nias.affrc.go.jp


Abstract:

The amount of mRNA of the Oryza sativa L., cv. Nipponbare (rice) catalase gene, CatB, was decreased in the roots of intact seedlings kept in continuous darkness (DD). In contrast, sense and antisense unspliced CatB transcripts accumulated in the same tissue. Both strands cover the entire CatB-coding region, and form double-stranded RNA (dsRNA). The results of RNA dot-blot hybridization analysis using low molecular weight RNAs suggested that the sense and antisense CatB transcripts were more stable under DD conditions than under a light–dark regimen (LD). After shifting the lighting conditions from DD to LD, both the sense and antisense CatB transcripts were hardly detected, and the amount of CatB mRNA was restored. From these results, the antisenseCatB transcripts might play a role in suppressing the normal processing of sense CatB transcript and also CatB protein synthesis by dsRNA formation, under conditions unsuitable for plant growth such as DD. This study indicates that signals transmitted from shoots are associated with the accumulation of sense and antisenseCatB transcripts in roots under DD conditions, and that auxin is one of the possible signals.

Abbreviations: cDNA, DNA complementary to RNA; dsRNA, double-stranded RNA; IAA, indole-3-acetic acid; LMW RNA, low molecular weight RNA; PCR, polymerase chain reaction; RT-PCR, reverse transcription polymerase chain reaction; Os, Oryza sativa; Cat, catalase; hox, homeodomain-leucine zipper transcription factor; ARF, auxin response factor; IAA, auxin-inducible; OSV, Oryza sativa endornavirus


Additional References:

1. Sun M, Hurst LD, Carmichael GG, and Chen J, "Evidence for variation in abundance of antisense transcripts between multicellular animals, but no relationship between antisense transcriptionand organismic complexity", Genome Research vol. 16: no. 7, pp. 922-933 (July, 2006).

2. Frenster JH, and Hovsepian JA, "Kissing Chromosomes and Paired Sense-Antisense RNA Synthesis". 71st Cold Spring Harbor Symposium on Quantitative Biology: Regulatory RNAs", Program page 62, May 31-June 5, 2006.

3. Xu N, Tsai C-L, and Lee JT, "Transient Homologous Pairing Marks the Onset of X Inactivation", Science vol. 311, no. 5764, pp. 1149-1152 (February 24, 2006).

4. Hovsepian JA, and Frenster JH, "Sense and Antisense during RNA Initiation of the DNA Transcription Bubble"., Presented at RNA2005, the Tenth Annual Meeting of the RNA Society, Banff, Alberta, Canada, May 24-29, 2005, and published in "RNA2005", p. 279, The RNA Society, Bethesda, MD 20814-3998, (2005).

5. Coudert AE, Pibouin L, Vi-Fane B, Thomas BL, Macdougall M, Choudhury A, Robert B, Sharpe PT, Berda A, and Lezot F, "Expression and regulation of the Msx1 natural antisense transcript during development", Nucleic Acid Research, vol. 33, no. 16, pp. 5208-5216 (2005).

6. Shin JT, Priest JR, Ovcharenko I, Ronco A, Moore RK, C. Burns CG, and MacRae CA,
"Human-zebrafish non-coding conserved elements act in vivo to regulate transcription".
 



 

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