ArticlePlant molecular biology1998
Isolation and characterization of two cyclin-like cDNAs from Arabidopsis.
Article in Plant molecular biology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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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.
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Who cites it
2 citing papers in PubMed, 16 citations in OpenAlex.
- Bacillus subtilis strain L1 promotes nitrate reductase activity in Arabidopsis and elicits enhanced growth performance in Arabidopsis, lettuce, and wheat.Journal of plant research · 2020Article
- Expression of cell cycle genes in shoot apical meristems.Plant molecular biology · 2006Review
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cyclins are key regulators of a family of protein kinases called cyclin-dependent kinases (Cdks). Specific cyclins interact with specific Cdks to regulate the different transition points in the cell cycle. Six mitotic-like cyclins have previously been reported in Arabidopsis thaliana. Using polymerase chain reaction amplified cyclin-box sequences as probes, two new cyclin cDNAs are isolated from Arabidopsis. The deduced amino acid sequences of the isolated cDNAs (Arath; CycB1;3 and Arath; CycB1;4) show the highest sequence similarity with mitotic cyclins. Arath; CycB1;3 is most homologous to the plant CycB1 group cyclins and contains a conserved motif that is typical of this group. Arath; CycB1;4, while homologous to Arath; CycB1;2, has some features that make it different from other known mitotic-like cyclins. These data suggest the presence of several distinct cyclins of CycB1 group in Arabidopsis. Analysis of expression of three members of CycB1 group (Arath; CycB1;2, Arath; CycB1;3 and Arath; CycB1;4) in different tissues by reverse transcription-polymerase chain reaction using primers corresponding to unique regions of their cDNAs shows that they are differentially expressed in different tissues.
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Registered trials
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