Evidence map›Paper›PMID 23277399›Full record

ArticleMolecular biology reports2013

Isolation and characterization of Histone1 gene and its promoter from tea plant (Camellia sinensis).

Wanping Fang, Yue Zhang, Lin Zhou, Weidong Wang, Xinghui Li

Abstract read
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Article in Molecular biology reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Application of Multi-Perspectives in Tea Breeding and the Main Directions.International journal of molecular sciences · 2023
    Review
  2. Article
  3. Article
  4. Insights into a key sulfite scavenger enzyme sulfite oxidase (Physiology and molecular biology of plants : an international journal of functional plant biology · 2017
    Article
  5. Article
4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Wanping FangTea Science Research Institute, Nanjing Agricultural University, Weigang No.1, Nanjing 210095, Jiangsu, People's Republic of China. fangwp@njau.edu.cn
Yue Zhang
Lin Zhou
Weidong Wang
Xinghui Li

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One 1.2 kbp long sequence was cloned by using PCR with primers that were designed from cDNA sequence of CsH1 gene (Genbank: EU716314) from tea plant (Camellia sinensis). According to the 1.2 kbp sequence, a 0.6 kbp sequence was isolated from tea plant genomic DNA using DNA Walking Method. Sequence analysis revealed that the 1.2 kbp sequence is a CsH1 gene consisting of 1 exon and 2 introns, the border of exton and intron sequences conforming to the GT-AG rule, and the 0.6 kbp sequence was found to be the promoter of CsH1 gene which contains basic promoter elements, TATA-box and CAAT-box. Abscisic acid responsiveness cis-acting element, elictor-responsive element, GA response element, light response cis-acting element and TC-rich repeats were also represented. To further study the activity of this promoter, the sequence was used to drive a GUS fusion gene in Agrobacterium-mediated transformation of tea plant somatic embryos, leaf discs and calli of tobacco (Nicotiana tabacum L.) where a high level of GUS expression was both observed in the tobacco calli and tea plant somatic embryos. These results suggest that the CsH1 gene promoter isolated is capable of conferring nuclear gene expression.

Indexed as

Promoter Regions, Genetic5' Flanking RegionAmino Acid SequenceBase SequenceCamellia sinensisCloning, MolecularGene ExpressionGene OrderGenetic VectorsHistonesMolecular Sequence DataPlant ProteinsSequence Analysis, DNAHistonesPlant Proteins

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.