Constans

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==Your Heading Here (maybe something like 'Structure')==
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==Structural highlights==
<StructureSection load='7VSQ ' size='340' side='right'caption='[[7VSQ]], [[Resolution|resolution]] 1.68&Aring;' scene=''>
<StructureSection load='7VSQ ' size='340' side='right'caption='[[7VSQ]], [[Resolution|resolution]] 1.68&Aring;' scene=''>
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This is a default text for your page '''Megi Celaj/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the &lt; and &gt; signs.
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Constans (CO) is composed of an N terminal that contains two Zinc finger domains known as B-boxes. Cysteine and histidine are the main coordinators of Zinc binding in this process. Mutations identified within the residues resulted in late flowering which is disadvantageous to reproduction patterns, and suggests they are highly conserved. B-boxes are involved in protein-protein interactions. The C-terminal contains 40 main amino acids (C-terminal contains 70-80 in entirety). In arabidopsis, 32 B-box transcription proteins have been identified thus far. CO, which is considered a BBX1, activates the expression of FT by binding to the CORE1 and CORE2 of the FT promoter. Each B-box transcription protein serves to regulate flowering by stimulating or repressing FT hormone. BBX28 is known to decrease FT transcription, specifically in the late afternoons and dark periods. BBX28 is able to interact with CO through the N-terminus. This works by decreasing recruitment of CO to the FT locus. Constans-like genes (COLs) are very genetically related homologs to Constans (CO). Specifically, CO1 has a greater than 80% amino acid genetic similarity to CO. While identity is similar, function of CO1 varys among identified organisms.
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You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.
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== Function ==
== Function ==
As flowers serve as the reproductive structure of all Angiosperms, the regulation of flowering plants is crucial in a plant’s survival and viability. CONSTANS (CO) serves as the key regulator protein of the photoperiodic flowering times of Arabidopsis (Arabidopsis thaliana). CONSTANS (CO) is able to modulate flowering times through the regulation of the florigen hormone FT (FLOWERING LOCUS T). CO regulation is incredibly specific to the growth stage, season, and time of day. In the presence of light stimulus, CO increases the production of FT (FLOWERING LOCUS T) which then begins the process of flower differentiation. Signals from the environment such as temperature and light availability can inversely act as inhibitors for FT. In complete darkness, CO is completely degraded and flowering is halted. Different lighting periods can result in varying accumulations of CO, which can reduce or increase the speed of flowering depending on light cues. Regulation of CO mRNA is controlled by the circadian rhythm of arabidopsis, particularly in enhancement of long days (LD). The nuclear protein GIGANTEA (GI) interacts with FLAVIN BINDING, KELCH REPEAT, F-BOX PROTEIN 1 (FKF1) to begin the degradation process with the use of DOF transcription factors known as Cycling Dof Factors (CDFs). CDFs are then able to bind to the CO promoter region and inhibit its expression during the morning, thus inhibiting flowering times. Since flowering times are incredibly specific, post translational CO activity is critical as peak mRNA expression is not necessarily concurrent with the exact time of CO activity. CO stability varies depending on light conditions. In the presence of blue light, CO stability is high as blue light impacts the photoreceptors PHYTOCHROME B (phyB) and CRYPTOCHROME 2 (CRY2). In red light, CO stability was poor as PHYB activity restricts flowering from occurring. Another key regulator of CO stability is proteasome. When there is darkness present and during the morning hours, proteasome works to degrade CO and thus prevent flowering from occurring. In light periods CO is stable and able to then activate FT to induce flowering.
As flowers serve as the reproductive structure of all Angiosperms, the regulation of flowering plants is crucial in a plant’s survival and viability. CONSTANS (CO) serves as the key regulator protein of the photoperiodic flowering times of Arabidopsis (Arabidopsis thaliana). CONSTANS (CO) is able to modulate flowering times through the regulation of the florigen hormone FT (FLOWERING LOCUS T). CO regulation is incredibly specific to the growth stage, season, and time of day. In the presence of light stimulus, CO increases the production of FT (FLOWERING LOCUS T) which then begins the process of flower differentiation. Signals from the environment such as temperature and light availability can inversely act as inhibitors for FT. In complete darkness, CO is completely degraded and flowering is halted. Different lighting periods can result in varying accumulations of CO, which can reduce or increase the speed of flowering depending on light cues. Regulation of CO mRNA is controlled by the circadian rhythm of arabidopsis, particularly in enhancement of long days (LD). The nuclear protein GIGANTEA (GI) interacts with FLAVIN BINDING, KELCH REPEAT, F-BOX PROTEIN 1 (FKF1) to begin the degradation process with the use of DOF transcription factors known as Cycling Dof Factors (CDFs). CDFs are then able to bind to the CO promoter region and inhibit its expression during the morning, thus inhibiting flowering times. Since flowering times are incredibly specific, post translational CO activity is critical as peak mRNA expression is not necessarily concurrent with the exact time of CO activity. CO stability varies depending on light conditions. In the presence of blue light, CO stability is high as blue light impacts the photoreceptors PHYTOCHROME B (phyB) and CRYPTOCHROME 2 (CRY2). In red light, CO stability was poor as PHYB activity restricts flowering from occurring. Another key regulator of CO stability is proteasome. When there is darkness present and during the morning hours, proteasome works to degrade CO and thus prevent flowering from occurring. In light periods CO is stable and able to then activate FT to induce flowering.
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== Structural highlights ==
 
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Constans (CO) is composed of an N terminal that contains two Zinc finger domains known as B-boxes. Cysteine and histidine are the main coordinators of Zinc binding in this process. Mutations identified within the residues resulted in late flowering which is disadvantageous to reproduction patterns, and suggests they are highly conserved. B-boxes are involved in protein-protein interactions. The C-terminal contains 40 main amino acids (C-terminal contains 70-80 in entirety). In arabidopsis, 32 B-box transcription proteins have been identified thus far. CO, which is considered a BBX1, activates the expression of FT by binding to the CORE1 and CORE2 of the FT promoter. Each B-box transcription protein serves to regulate flowering by stimulating or repressing FT hormone. BBX28 is known to decrease FT transcription, specifically in the late afternoons and dark periods. BBX28 is able to interact with CO through the N-terminus. This works by decreasing recruitment of CO to the FT locus. Constans-like genes (COLs) are very genetically related homologs to Constans (CO). Specifically, CO1 has a greater than 80% amino acid genetic similarity to CO. While identity is similar, function of CO1 varys among identified organisms.
 
== Relevance ==
== Relevance ==
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== References ==
== References ==
<references/>
<references/>
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3. Federico Valverde, CONSTANS and the evolutionary origin of photoperiodic timing of flowering, Journal of Experimental Botany, Volume 62, Issue 8, May 2011, Pages 2453–2463, https://doi.org/10.1093/jxb/erq449
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3. Federico Valverde, CONSTANS and the evolutionary origin of photoperiodic timing of flowering, Journal of Experimental Botany, Volume 62, Issue 8, May 2011, Pages 2453–2463, https://doi.org/10.1093/jxb/erq449
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4. Khanna, Rajnish et al. “The Arabidopsis B-box zinc finger family.” The Plant cell vol. 21,11 (2009): 3416-20. doi:10.1105/tpc.109.069088
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4. Khanna, Rajnish et al. “The Arabidopsis B-box zinc finger family.” The Plant cell vol. 21,11 (2009): 3416-20. doi:10.1105/tpc.109.069088
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5. Kim, S. Y., Yu, X., & Michaels, S. D. (2008). Regulation of CONSTANS and FLOWERING LOCUS T expression in response to changing light quality. Plant physiology, 148(1), 269–279. https://doi.org/10.1104/pp.108.122606
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5. Kim, S. Y., Yu, X., & Michaels, S. D. (2008). Regulation of CONSTANS and FLOWERING LOCUS T expression in response to changing light quality. Plant physiology, 148(1), 269–279. https://doi.org/10.1104/pp.108.122606
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6. Liu, Y., Lin, G., Yin, C. et al. B-box transcription factor 28 regulates flowering by interacting with constans. Sci Rep 10, 17789 (2020). https://doi.org/10.1038/s41598-020-74445-7
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6. Liu, Y., Lin, G., Yin, C. et al. B-box transcription factor 28 regulates flowering by interacting with constans. Sci Rep 10, 17789 (2020). https://doi.org/10.1038/s41598-020-74445-7

Revision as of 19:06, 29 April 2022

Structural highlights

PDB ID 7VSQ

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References

       3. Federico Valverde, CONSTANS and the evolutionary origin of photoperiodic timing of flowering, Journal of Experimental Botany, Volume 62, Issue 8, May 2011, Pages 2453–2463, https://doi.org/10.1093/jxb/erq449
       4. Khanna, Rajnish et al. “The Arabidopsis B-box zinc finger family.” The Plant cell vol. 21,11 (2009): 3416-20. doi:10.1105/tpc.109.069088
       5. Kim, S. Y., Yu, X., & Michaels, S. D. (2008). Regulation of CONSTANS and FLOWERING LOCUS T expression in response to changing light quality. Plant physiology, 148(1), 269–279. https://doi.org/10.1104/pp.108.122606
       6. Liu, Y., Lin, G., Yin, C. et al. B-box transcription factor 28 regulates flowering by interacting with constans. Sci Rep 10, 17789 (2020). https://doi.org/10.1038/s41598-020-74445-7

Proteopedia Page Contributors and Editors (what is this?)

Megi Celaj, Michal Harel, Jason Telford, Jaime Prilusky

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