Faculty Opinions recommendation of Sequence and analysis of rice chromosome 4.

Author(s):  
Klaus Mayer
Keyword(s):  
Genetica ◽  
2010 ◽  
Vol 138 (11-12) ◽  
pp. 1277-1296 ◽  
Author(s):  
Tong Geon Lee ◽  
Yong Jin Lee ◽  
Dae Yeon Kim ◽  
Yong Weon Seo

2013 ◽  
Vol 3 (1) ◽  
Author(s):  
Yusaku Uga ◽  
Eiji Yamamoto ◽  
Noriko Kanno ◽  
Sawako Kawai ◽  
Tatsumi Mizubayashi ◽  
...  

2001 ◽  
Vol 11 (7) ◽  
pp. 1167-1174
Author(s):  
Klaus Mayer ◽  
George Murphy ◽  
Renato Tarchini ◽  
Rolf Wambutt ◽  
Guido Volckaert ◽  
...  

The nucleotide sequence was determined for a 340-kb segment of rice chromosome 2, revealing 56 putative protein-coding genes. This represents a density of one gene per 6.1 kb, which is higher than was reported for a previously sequenced segment of the rice genome. Sixteen of the putative genes were supported by matches to ESTs. The predicted products of 29 of the putative genes showed similarity to known proteins, and a further 17 genes showed similarity only to predicted or hypothetical proteins identified in genome sequence data. The region contains a few transposable elements: one retrotransposon, and one transposon. The segment of the rice genome studied had previously been identified as representing a part of rice chromosome 2 that may be homologous to a segment of Arabidopsis chromosome 4. We confirmed the conservation of gene content and order between the two genome segments. In addition, we identified a further four segments of the Arabidopsis genome that contain conserved gene content and order. In total, 22 of the 56 genes identified in the rice genome segment were represented in this set of Arabidopsis genome segments, with at least five genes present, in conserved order, in each segment. These data are consistent with the hypothesis that theArabidopsis genome has undergone multiple duplication events. Our results demonstrate that conservation of the genome microstructure can be identified even between monocot and dicot species. However, the frequent occurrence of duplication, and subsequent microstructure divergence, within plant genomes may necessitate the integration of subsets of genes present in multiple redundant segments to deduce evolutionary relationships and identify orthologous genes.


2008 ◽  
Vol 1 (5) ◽  
pp. 816-829 ◽  
Author(s):  
Ben-Liang Yin ◽  
Lan Guo ◽  
Dong-Fen Zhang ◽  
William Terzaghi ◽  
Xiang-Feng Wang ◽  
...  

Nature ◽  
2002 ◽  
Vol 420 (6913) ◽  
pp. 316-320 ◽  
Author(s):  
Qi Feng ◽  
Yujun Zhang ◽  
Pei Hao ◽  
Shengyue Wang ◽  
Gang Fu ◽  
...  
Keyword(s):  

2002 ◽  
Vol 12 (5) ◽  
pp. 817-823 ◽  
Author(s):  
Q. Zhao

2021 ◽  
Vol 22 (14) ◽  
pp. 7593
Author(s):  
Manatchanok Kongdin ◽  
Bancha Mahong ◽  
Sang-Kyu Lee ◽  
Su-Hyeon Shim ◽  
Jong-Seong Jeon ◽  
...  

Conjugation of phytohormones with glucose is a means of modulating their activities, which can be rapidly reversed by the action of β-glucosidases. Evaluation of previously characterized recombinant rice β-glucosidases found that nearly all could hydrolyze abscisic acid glucose ester (ABA-GE). Os4BGlu12 and Os4BGlu13, which are known to act on other phytohormones, had the highest activity. We expressed Os4BGlu12, Os4BGlu13 and other members of a highly similar rice chromosome 4 gene cluster (Os4BGlu9, Os4BGlu10 and Os4BGlu11) in transgenic Arabidopsis. Extracts of transgenic lines expressing each of the five genes had higher β-glucosidase activities on ABA-GE and gibberellin A4 glucose ester (GA4-GE). The β-glucosidase expression lines exhibited longer root and shoot lengths than control plants in response to salt and drought stress. Fusions of each of these proteins with green fluorescent protein localized near the plasma membrane and in the apoplast in tobacco leaf epithelial cells. The action of these extracellular β-glucosidases on multiple phytohormones suggests they may modulate the interactions between these phytohormones.


2011 ◽  
Vol 2011 ◽  
pp. 1-11 ◽  
Author(s):  
Eiko Himi ◽  
Masahiko Maekawa ◽  
Kazuhiko Noda

Flavonoid pigments are known to accumulate in red grains and coleoptiles of wheat and are synthesized through the flavonoid biosynthetic pathway. Flavanone 3-hydroxylase (F3H) is a key enzyme at a diverging point of the flavonoid pathway leading to production of different pigments: phlobaphene, proanthocyanidin, and anthocyanin. We isolated three F3H genes from wheat and examined a relationship between their expression and tissue pigmentation. Three F3Hs are located on the telomeric region of the long arm of chromosomes 2A, 2B, and 2D, respectively, designated as F3H-A1, F3H-B1, and F3H-D1. The telomeric regions of the long arms of the chromosomes of homoeologous group 2 of wheat showed a syntenic relationship to the telomeric region of the long arm of rice chromosome 4, on which rice F3H gene was also located. All three genes were highly activated in the red grains and coleoptiles and appeared to be controlled by flavonoid regulators in each tissue.


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