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Cryptochrome

Cryptochromes are flavoproteins that function as blue-light photoreceptors in a wide range of organisms, including plants, animals, fungi, and bacteria, and are structurally related to DNA photolyases but lack DNA repair activity.^[1] These proteins contain a flavin adenine dinucleotide (FAD) chromophore that enables them to absorb blue light (approximately 350–500 nm) and undergo photo-induced electron transfer, leading to the formation of radical pairs that transduce light signals into biological responses.^[2] First discovered in the plant Arabidopsis thaliana in 1993, cryptochromes were identified through genetic screens for mutants defective in blue-light-mediated inhibition of hypocotyl elongation, with CRY1 and CRY2 as the primary isoforms in plants.^[1] In animals, homologs such as those in Drosophila and mammals were characterized in the late 1990s, revealing their conserved roles despite evolutionary divergence.^[2] In plants, cryptochromes primarily regulate photomorphogenesis, the light-dependent development processes that control seedling growth, stem elongation, leaf expansion, and floral initiation.^[1] For instance, in Arabidopsis, CRY1 mediates sustained blue-light responses, while CRY2 handles short-term signaling, influencing up to 10–20% of the genome through interactions with transcription factors like PIFs and modulation of chromatin dynamics via histone variant deposition.^[2] They also entrain the circadian clock by perceiving blue light to adjust the period and phase of rhythms, ensuring synchronization with daily light-dark cycles, and contribute to stress responses such as viral defense and stomatal regulation.^[2] Evolutionarily, plant cryptochromes trace back to algal ancestors, with CRY1 present across all plant phyla and CRY2 emerging in flowering plants.^[2] In animals, cryptochromes play dual roles in circadian regulation and sensory perception. In mammals, CRY1 and CRY2 act as transcriptional repressors in the molecular clock, inhibiting CLOCK-BMAL1 activity in a light-independent manner within the suprachiasmatic nucleus, though they lack direct photoreceptive function in this context.^[3] In contrast, Drosophila CRY serves as a light-dependent circadian photoreceptor, promoting degradation of TIM protein to reset the clock.^[1] A particularly notable function is their proposed involvement in magnetoreception, especially in birds, where CRY4a in retinal double cones and long-wavelength single cones forms light-induced radical pairs sensitive to the geomagnetic field's inclination, enabling navigational orientation during migration.^[4]^[5] This radical pair mechanism, disrupted by radiofrequency fields around 7 MHz, provides evidence for cryptochromes as the molecular basis of the avian magnetic compass, though it requires blue or UV light activation and operates in the dark phase of the photocycle.^[4]

Introduction

Definition and Properties

Cryptochromes are flavin-based photoreceptor proteins that function as non-enzymatic signaling molecules, primarily sensitive to blue light in the 400-500 nm range and ultraviolet-A (UV-A) wavelengths.^[6] These proteins bind flavin adenine dinucleotide (FAD) as their chromophore and mediate light-dependent biological responses by undergoing photoinduced conformational changes.^[7] Key properties of cryptochromes include high photostability, allowing repeated light exposure without degradation of the protein or cofactor, and the capacity for reversible redox cycles. Upon absorbing a blue photon, the oxidized FAD (FAD_ox) transitions to a neutral semiquinone radical (FADH•) state, which serves as the primary signaling intermediate:

h\nu + \text{CRY(FAD}_{\text{ox}}\text{)} \rightarrow \text{CRY(FADH•)}

where h\nu represents the energy of a blue photon.^[6] This process exhibits a quantum yield of approximately 0.2-0.3 for formation of the signaling state. The semiquinone radical state thermally reverts to the oxidized form with half-lives ranging from minutes to hours, varying by species and conditions; for instance, in Arabidopsis thaliana cryptochromes, half-lives are about 5 minutes for CRY1 and 16 minutes for CRY2.^[8]^[9] In general, cryptochromes act as light-dependent regulators of development, timing, and environmental sensing across kingdoms, with evolutionary conservation tracing back to bacterial ancestors and presence in diverse organisms such as Arabidopsis, Drosophila, and humans.^[6]

Classification and Occurrence

Cryptochromes are classified into four major groups based on phylogenetic analyses and structural features: plant cryptochromes (pCRY), animal cryptochromes (aCRY), bacterial cryptochromes (bCRY), and cryptochrome DASH (CRY-DASH).^[1] These classes share a conserved photolyase homology region (PHR) that binds flavin adenine dinucleotide (FAD) but diverge in their C-terminal extensions and functions.^[10] Plant cryptochromes, such as CRY1 and CRY2 in Arabidopsis thaliana, feature extended C-terminal domains that promote nuclear localization and are involved in light signaling.^[1] Animal cryptochromes, exemplified by CRY1 and CRY2 in mammals, possess shorter C-terminal tails and function primarily as transcriptional repressors in circadian regulation.^[11] Bacterial cryptochromes are typically shorter, lacking C-terminal domains, and are found in prokaryotes like cyanobacteria.^[1] CRY-DASH proteins, also known as CRY3, resemble DNA photolyases with residual repair activity for cyclobutane pyrimidine dimers but lack C-terminal extensions.^[10] Cryptochromes occur widely across phylogenetic lineages but are absent in certain groups, such as some fungi and nematodes.^[12] They are ubiquitous in plants, most animals (including humans, where CRY1—UniProt Q16526, gene ID 1407—and CRY2—gene ID 1409—are encoded), cyanobacteria (e.g., Synechocystis sp.), and protists like Chlamydomonas reinhardtii.^[10] In vertebrates, gene duplication events have produced CRY1 and CRY2 paralogs, with the human proteins sharing a conserved FAD-binding motif despite approximately 48% overall sequence identity.^[11]^[13]

Discovery and Evolutionary History

Discovery

The isolation of the hy4 mutant in Arabidopsis thaliana in 1980 marked a pivotal step in identifying a blue light-specific signaling pathway distinct from that mediated by phytochromes. This mutant, characterized by defective inhibition of hypocotyl elongation under blue light, was obtained through genetic screening by Maarten Koornneef and colleagues, revealing a photoreceptor pathway insensitive to red or far-red light.^[14] In 1993, the HY4 gene underlying the hy4 mutation was cloned, encoding a protein with significant sequence homology to DNA photolyases from Escherichia coli, suggesting a flavin-based blue light photoreceptor function. This discovery, reported by Mohamed Ahmad and Anthony R. Cashmore, established cryptochrome 1 (CRY1) as the product of HY4 and provided the first molecular insight into blue light perception in plants.^[15] The identification of cryptochromes extended to animals in the late 1990s. In mice, CRY1 was discovered in 1997 through sequence homology searches, with subsequent knockout studies in 1998 revealing its involvement in circadian regulation, as evidenced by altered light-induced phase shifts in locomotor activity; however, mammalian cryptochromes function primarily as transcriptional repressors in the clock mechanism rather than direct photoreceptors.^[16] Similarly, in Drosophila melanogaster, the dCRY gene was identified in 1998 by Paul Emery and colleagues via a mutation screen; the cry^b mutant exhibited severe defects in circadian rhythm resetting by light, confirming dCRY as a dedicated circadian photoreceptor.^[16] Key milestones included the 2003 spectroscopic confirmation of flavin adenine dinucleotide (FAD) as the chromophore in Arabidopsis cryptochrome 3 (At-CRY3), a homolog of Synechocystis cryptochrome, through absorption spectra matching authentic FAD after chromophore release. Additionally, early 2000s genome projects revealed bacterial orthologs, such as the cryptochrome in Synechocystis sp. PCC6803, characterized in 2000 as a photolyase-like protein binding FAD non-covalently but lacking DNA repair activity.^[17]^[18]

Evolutionary History

Cryptochromes trace their evolutionary origins to approximately 3.5 billion years ago, emerging from type II cyclobutane pyrimidine dimer (CPD) photolyases in ancient prokaryotes under conditions of intense ultraviolet radiation. These early proteins functioned primarily in DNA repair, utilizing blue light to reverse UV-induced damage, but over time, cryptochromes diverged by losing this repair capability while acquiring novel signaling roles through the addition of C-terminal extensions that facilitate interactions with regulatory proteins and subcellular localization. Recent studies (as of 2021) have identified novel ancestral classes, such as iron-sulfur bacterial cryptochromes and photolyases (FeS-BCPs), supporting prokaryotic origins and multiple horizontal gene transfer (HGT) events.^[19]^[20] The divergence of cryptochrome lineages reflects distinct evolutionary trajectories across domains of life. Bacterial cryptochromes (bCRY) retained relatively simple functions, often linked to basic photoreception or residual repair activities, serving as the basal outgroup in phylogenetic analyses. In plants, plant cryptochromes (pCRY) evolved in the Paleozoic Era (approximately 541–252 million years ago), likely through horizontal gene transfer (HGT) from bacterial sources, enabling adaptation to light-mediated growth and development. Animal cryptochromes (aCRY), in contrast, arose approximately 600 million years ago in the common ancestor of bilaterians during the Neoproterozoic Era, with subsequent duplications in vertebrates—such as the CRY1/CRY2 split around 500 million years ago in the Silurian-Devonian period—facilitating specialized roles in circadian regulation; note that the CRY1/CRY2 duplication predates the arthropod-vertebrate divergence in some lineages. Sequence phylogenies consistently position bCRY as the outgroup to both pCRY and aCRY clades, underscoring ancient HGT events from bacteria to eukaryotic lineages as a key mechanism in cryptochrome diversification.^[21]^[22]^[23]^[24] Lineage-specific losses and retentions highlight the dynamic evolution of cryptochromes. For instance, cryptochromes are absent in nematodes like Caenorhabditis elegans due to secondary loss in the Ecdysozoa clade, reflecting reduced selective pressure in certain environments. Conversely, their presence in diverse phyla such as mollusks and birds, where they contribute to magnetosensing capabilities, exemplifies convergent evolution for environmental orientation, with independent adaptations in non-vertebrate and vertebrate lineages.^[19]^[19]

Molecular Structure

Overall Architecture

Cryptochrome proteins are typically composed of 500 to 700 amino acids, with variations depending on the organism and subtype.^[25]^[26] The core structural element is the photolyase homology region (PHR), which spans approximately 350 to 500 amino acids and exhibits a high degree of evolutionary conservation across plants, animals, and microorganisms. This region folds into an α/β/α sandwich structure, featuring 8 to 11 β-strands arranged in a central sheet and around 20 α-helices that form the scaffold, thereby enclosing a pocket for the flavin cofactor.^[27]^[28] The PHR is subdivided into an N-terminal α/β domain, characterized by a Rossmann-like fold with parallel β-strands flanked by helices, and a C-terminal helical domain that contributes additional α-helices to cap the cofactor-binding site.^[29] Adjacent to the PHR lies the C-terminal domain (CCT), which measures approximately 100 to 180 amino acids in plant cryptochromes (pCRY), such as 110 aa in Arabidopsis CRY2 and 180 aa in CRY1, and 20 to 50 amino acids in many animal cryptochromes (aCRY), but is either absent or significantly shorter in bacterial cryptochromes (bCRY).^[30] In plants, the CCT incorporates nuclear localization signals (NLS) that facilitate translocation to the nucleus, while in animals, it contains a conserved DQXVP motif (often referred to as the DAS domain) implicated in protein dimerization and interactions with circadian clock components.^[12] The CCT is generally intrinsically disordered, allowing flexibility for signaling roles, though it varies widely in sequence and length across cryptochrome classes.^[31] Regarding oligomerization, cryptochromes predominantly exist as monomers in solution in the dark, as observed in biochemical assays, but crystal structures frequently reveal dimeric assemblies, and oligomerization is often light-dependent. For instance, Arabidopsis CRY1 undergoes sequential monomer-to-dimer-to-tetramer transitions upon blue light illumination.^[32]^[33] The crystal structure of Arabidopsis thaliana CRY2 (PDB ID: 6K8I) displays an antiparallel dimer interface mediated by the PHR domains, highlighting potential regulatory contacts at the protein surface.^[34] The helical cap domain within the PHR, formed by a cluster of α-helices overlying the flavin pocket, plays a key role in stabilizing the flavin semiquinone radical intermediate essential for light sensing.^[27] Recent high-resolution structures, including cryo-EM models of cryptochrome PHR domains and complexes at resolutions around 3 Å (e.g., Arabidopsis CRY2-CIB1), have revealed conformational changes in the PHR for downstream interactions.^[35]

Chromophores and Cofactors

Cryptochromes contain flavin adenine dinucleotide (FAD) as their primary chromophore, which is bound non-covalently within the photolyase homology region (PHR) pocket. This cofactor is essential for light absorption and is present in the oxidized state (FAD^ox) in the dark-adapted form of the protein. The oxidized FAD exhibits an absorption maximum at approximately 450 nm, enabling sensitivity to blue light.^[36]^[37] Upon illumination, FAD undergoes redox changes to form semiquinone radicals, including the anionic semiquinone (FAD^•−) with an absorption maximum around 590 nm and the neutral semiquinone (FADH^•) absorbing at about 360 nm, which serves as a key signaling intermediate. Unlike photolyases, most cryptochromes do not achieve full reduction to FADH₂, limiting their catalytic repair activity and instead facilitating signaling roles. These redox states are stabilized by the protein environment, with FAD^ox predominant in darkness and FAD^•− accumulating under light exposure in some cryptochromes.^[38]^[29] Antenna pigments enhance light harvesting by transferring excitation energy to FAD. In plant and bacterial cryptochromes, 5,10-methenyltetrahydrofolate (MTHF) acts as this secondary chromophore, absorbing maximally near 380 nm with a molar extinction coefficient of 25,000 M⁻¹cm⁻¹ and efficiently funneling energy via Förster resonance energy transfer. Recent NMR studies on Arabidopsis CRY1 reveal an MTHF-FAD distance of approximately 10 Å, supporting up to 90% energy transfer efficiency due to optimal orientation and proximity.^[39]^[40] In certain animal cryptochromes, 8-hydroxy-7,8-didemethyl-5-deazariboflavin (8-HDF, also known as F₀) has been proposed as an alternative antenna pigment, broadening the spectral range for excitation transfer to FAD and potentially aiding specialized functions like magnetoreception. This cofactor binds similarly non-covalently and contributes to the photochemical versatility across cryptochrome variants.^[41]

Mechanisms of Action

Light Absorption and Photochemistry

Cryptochromes primarily absorb blue light via their conserved flavin adenine dinucleotide (FAD) chromophore, which is present in oxidized form (FAD^{\rm ox}) across plant, animal, and microbial classes.^[42] Upon blue light absorption, FAD^{\rm ox} undergoes intersystem crossing to its triplet excited state (^3FAD*), with a lifetime of approximately 0.5 ms, before rapid electron transfer occurs from a conserved tryptophan (Trp) triad. In Arabidopsis cryptochrome 1, this triad consists of W400, H378, and W324, enabling sequential electron donation that generates a semiquinone anion radical (FAD^{\bullet -}) and a neutral Trp radical (Trp^{\bullet}). The process involves proton-coupled electron transfer (PCET), represented by the key reaction:

^3\text{FAD}^* + \text{TrpH} \to \text{FAD}^{\bullet -} + \text{Trp}^{\bullet} + \text{H}^+

This PCET is facilitated by a nearby aspartate residue (e.g., D396 in Arabidopsis), which experiences a pKa shift of approximately 5 units to promote proton donation and stabilize the radical intermediates.^[43]^[44] The resulting radical pair is spin-correlated in its initial singlet state, undergoing singlet-triplet mixing due to hyperfine interactions, which underlies potential magnetic sensitivity. In the absence of light, the pair recombines or undergoes thermal reoxidation by molecular oxygen, reverting to FAD^{\rm ox} on timescales of seconds to minutes. The quantum yield for forming the long-lived signaling state (semireduced FADH^{\bullet}) is approximately 0.15, as determined for Arabidopsis cryptochrome 2 under physiological conditions.^[45] Recent hydrogen-deuterium exchange mass spectrometry (HDX-MS) studies from 2025 on Drosophila cryptochrome demonstrate conformational stiffening in the radical state within 10 ms post-illumination, reflecting rapid structural adjustments in the C-terminal domain that support signaling initiation.^[46]

Signal Transduction Pathways

Upon photoactivation, cryptochromes undergo conformational changes driven by the long-lived flavin semiquinone radical pair, which exposes the C-terminal tail (CCT) and initiates downstream signaling.^[38] This exposure facilitates phosphorylation of the CCT, such as by photoregulatory protein kinases (PPKs) in plants, which enhances cryptochrome activity and photobody formation.^[47] In certain contexts, the activated form also confers resistance to ubiquitination, prolonging its functional lifetime.^[48] Dimerization of photoactivated cryptochromes promotes efficient signal propagation by stabilizing oligomeric states necessary for partner recruitment. Binding to regulatory partners, such as 14-3-3 proteins, further stabilizes the active conformation and modulates interactions within signaling complexes.^[49] Recent investigations highlight light-induced liquid-liquid phase separation (LLPS) in CRY2, mediated by its intrinsically disordered region (IDR), which forms dynamic droplets that recruit m⁶A RNA methyltransferases to regulate mRNA methylation and stability.^[50] In general signaling pathways, photoactivated cryptochromes (photo-CRYs) inhibit E3 ubiquitin ligases, such as COP1 in plants, thereby preventing the degradation of transcription factors like HY5 and promoting photomorphogenic responses.^[51] In animals, cryptochromes form complexes with clock proteins such as PER and TIM, facilitating their nuclear import to repress core clock genes like per and tim (in Drosophila) or interact with CLOCK-BMAL1 complexes (in mammals) to inhibit transcription.^[52] These mechanisms underscore the role of post-translational modifications in fine-tuning cryptochrome-mediated responses. Recent developments in targeted protein degradation, including PROTACs specific to CRY1 and CRY2, highlight the role of ubiquitination and proteasomal pathways in regulating their stability.^[53]

Biological Functions

In Plants

In plants, cryptochromes (CRYs) primarily mediate blue light-induced photomorphogenesis, the developmental transition from dark-grown etiolated seedlings to light-adapted forms. Arabidopsis CRY1 and CRY2 inhibit the COP1 E3 ubiquitin ligase upon blue light activation, thereby stabilizing the transcription factor HY5 and preventing its degradation; this promotes de-etiolation responses such as chloroplast development, anthocyanin accumulation, and inhibition of hypocotyl elongation. The hy4 mutant, which lacks functional CRY1, displays long hypocotyls and reduced de-etiolation under blue light, underscoring CRY1's essential role in these processes.^[15] A brief blue light pulse of 1 µmol/m² activates CRY1 within 5 minutes, leading to peak HY5 mRNA accumulation at 30 minutes and subsequent gene expression changes that drive photomorphogenesis.^[54] CRYs also regulate phototropism, the directional growth toward blue light, by establishing asymmetric auxin distribution in Arabidopsis hypocotyls. Activated CRY1 triggers the relocation of PIN1 auxin efflux carriers to the plasma membrane on the illuminated side, facilitating auxin accumulation on the shaded side and promoting differential cell elongation for first positive phototropism.^[54] This CRY-mediated auxin asymmetry integrates with general signal transduction pathways, such as COP1 inhibition, to fine-tune tropic responses without overlapping broader structural mechanisms. Beyond core developmental roles, CRYs influence stomatal physiology and shade responses. In guard cells, blue light-activated CRY1 inhibits COP1 to promote stomatal opening, enhancing CO₂ uptake and photosynthesis while balancing water loss.^[55] For shade avoidance, CRY1 promotes the degradation of the PIF3 transcription factor under blue light, counteracting shade-induced elongation and favoring photomorphogenic growth in low-red/far-red environments.^[54] Recent research further reveals that photoexcited CRY2 undergoes liquid-liquid phase separation (LLPS) to form condensates with SPA1 and FIO1, regulating RNA alternative splicing and influencing hypocotyl elongation during light responses.^[56]

In Animals

In animals, cryptochromes (CRYs) play pivotal roles in circadian rhythm entrainment and sensory processes, particularly through light-dependent interactions that regulate molecular clocks and behavioral responses. In Drosophila melanogaster, the animal cryptochrome dCRY acts as a photoreceptor that binds to the clock protein Timeless (TIM) upon blue light exposure, triggering TIM's ubiquitination and proteasomal degradation, which resets the circadian oscillator and entrains the clock to environmental light-dark cycles.^[57] This light-induced degradation prevents premature clock resetting and ensures proper ~24-hour periodicity.^[58] In mammals, CRY1 and CRY2 function as nuclear transcriptional repressors within the core circadian feedback loop, where they form complexes with Period (PER) proteins to inhibit the activity of the CLOCK:BMAL1 heterodimer at E-box promoters, thereby repressing Per and Cry gene expression and maintaining oscillatory rhythms with a period of approximately 24 hours.^[59] Recent studies on subterranean rodents, such as blind mole rats, have identified recurrent mutations in Cry1, including alterations that disrupt clock gene expression in the liver and extend the intrinsic period (tau) beyond typical values, adapting circadian timing to perpetual darkness.^[60] Beyond timing, CRYs contribute to non-visual photic responses in the retina. In mice, cryptochromes in the retina contribute to the pupillary light reflex (PLR), mediating pupil constriction in response to light independently of image-forming vision; knockout of Cry1 and Cry2 significantly reduces PLR amplitude, particularly under dim blue light conditions.^[61] Cryptochromes also underlie magnetoreception in migratory birds, where retinal CRY4 is proposed to form light-induced radical pairs involving FAD and tryptophan residues sensitive to the geomagnetic field (~50 µT), enabling compass orientation during migration.^[62] Disruption of CRY function has notable health implications, linking circadian misalignment to disorders like sleep disturbances and cancer. For instance, in 2025 preclinical models of glioma, the CRY2 activator SHP1705 sensitizes glioblastoma stem cells to therapy by targeting hijacked clock machinery, reducing tumor viability while showing safety in Phase I trials.^[63] Chronic CRY deficiency, as observed in knockout models, enhances basal antiviral defenses by upregulating type I interferon (IFN) effectors and restricting influenza A virus replication through proteotoxic stress pathways.^[64] In human fibroblasts with CRY1 knockout, exposure to 10 µM blue light induces rapid desynchronization of circadian oscillations, with rhythm amplitude dropping by more than 50%, underscoring CRY1's role in photic robustness.^[65]

In Microorganisms

Cryptochromes in microorganisms primarily encompass bacterial cryptochromes (bCRYs) and DASH-type variants, which differ from the signaling roles in higher eukaryotes by focusing on DNA repair and environmental adaptation in unicellular contexts.^[28] In cyanobacteria, such as Synechocystis sp. PCC 6803, the DASH cryptochrome encoded by the sll1629 gene plays a critical role in maintaining photosynthetic efficiency through DNA repair. This protein facilitates the repair of cyclobutane pyrimidine dimers in single-stranded DNA, specifically supporting the recovery and function of Photosystem II under blue light exposure, thereby preventing photodamage to photosynthetic machinery.^[66] Protists like the green alga Chlamydomonas reinhardtii express an animal-like cryptochrome (aCRY) that exhibits bifunctional activity, combining blue light sensing with DNA repair capabilities. The crystal structure of CraCRY, resolved in 2018, reveals an active site configured for repairing (6-4) photoproducts in DNA lesions in vitro, highlighting its role in UV protection and genomic stability in this photosynthetic protist.^[67] In the fungus Aspergillus nidulans, a model microorganism, the photolyase-like cryptochrome CryA integrates light perception with developmental regulation. CryA governs asexual conidiation and sexual development in response to blue and UV-A light, with mutants showing altered spore formation and heightened sensitivity to oxidative stress, underscoring its contribution to light-mediated stress responses and reproduction.^[68]^[69] Recent investigations into bacterial pathogens reveal connections between cryptochrome/photolyase family members and virulence modulation under light conditions. For instance, in the plant pathogen Pseudomonas cichorii, a photolyase homolog enhances tolerance to environmental stresses and promotes virulence factors, suggesting a broader role for these flavoproteins in light-regulated pathogenicity in prokaryotes.^[70]

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Molecular basis for blue light-dependent phosphorylation of ... - Nature
May 11, 2017 · Cryptochrome phosphorylation has been extensively ... Consistent with CRY2 phosphorylation in plants, PPK-catalysed CRY2 phosphorylation ...
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Regulation of Arabidopsis photoreceptor CRY2 by two distinct E3 ...
Apr 12, 2021 · Like animal CRYs, the abundance and overall cellular activity of plant CRYs are regulated by phosphorylation, ubiquitination, and proteolysis.
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Signaling Mechanisms by Arabidopsis Cryptochromes - Frontiers
The idea of CRY2 binding DNA is conceivable, as CRYs have evolved from ancestral photolyases that bind pyrimidine dimers in the DNA. In line with this, the ...<|separator|>
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Cryptochrome 2 competes with COP1 substrates to repress ... - PNAS
Dec 10, 2019 · ... cryptochrome carboxyl terminus (CCT) (31). PHR is the chromophore ... exposure to blue light (50 µmol m-2 s-1) (blue) for 3 h. Error ...Sign Up For Pnas Alerts · Results · Cry2 With A Mutated Vp Motif...
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KPNB1 mediates PER/CRY nuclear translocation and circadian ...
Aug 29, 2015 · These data show that KPNB1 is required for timely nuclear import of PER/CRY in the negative feedback regulation of the circadian clock.
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Development of compounds for targeted degradation of mammalian ...
Jan 23, 2025 · The mammalian cryptochrome proteins (CRY1 and CRY2) are transcriptional repressors most notable for their role in circadian transcriptional ...Abstract · Introduction · Results · Discussion
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Mechanisms of Cryptochrome-Mediated Photoresponses in Plants
Apr 29, 2020 · This article discusses the mechanisms of cryptochrome-mediated photoresponses in plants, by Qin Wang and Chentao Lin.<|control11|><|separator|>
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Arabidopsis COP1 guides stomatal response in guard cells through ...
Feb 5, 2024 · Arabidopsis COP1 is a central light signaling repressor that suppresses stomatal opening in guard cells by inhibiting light-induced opening and ...
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Light-induced LLPS of the CRY2/SPA1/FIO1 complex regulating ...
Dec 8, 2023 · Arabidopsis CRY2 is a nuclear photoreceptor that undergoes light-induced homo-oligomerization and liquid–liquid phase separation (LLPS) to ...
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Cryptochrome-Timeless structure reveals circadian clock timing ...
... Cryptochrome (Cry) entrains the clock by triggering Tim degradation in light2,3. Here, through cryogenic electron microscopy of the Cry-Tim complex, we show ...
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Veela defines a molecular link between Cryptochrome and Timeless ...
Nov 14, 2006 · This light-induced degradation of Tim is crucial for molecular and behavioral clock resetting. If Tim is degraded prematurely by light ...
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Dual modes of CLOCK:BMAL1 inhibition mediated by Cryptochrome ...
Ye et al. show that CRY binds to CLOCK–BMAL1 at the promoter and inhibits CLOCK–BMAL1-dependent transcription without dissociating the complex.
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A repeatedly evolved mutation in Cryptochrome-1 of subterranean ...
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Reduced pupillary light responses in mice lacking cryptochromes
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The Magnetic Compass of Birds: The Role of Cryptochrome - Frontiers
Here, we will focus on the avian magnetic compass, its functional properties and what is presently known about the detection of magnetic directional information ...Missing: magnetosensing mollusks convergent<|control11|><|separator|>
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Light-induced conformational switching and magnetic sensitivity of ...
... cryptochrome undergoes upon blue light exposure ... ∙ Fingerhut, B.P.. Regulatory impact of the C-terminal tail on charge transfer pathways in Drosophila ...
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Evaluating SHP1705 CRY2 Activator Efficacy in Preclinical Models ...
Apr 1, 2025 · SHP1705 is the first circadian clock-modulating compound to be found safe and well-tolerated in Phase I clinical trials.Missing: disruption sleep disorders cancer
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Chronic CRYPTOCHROME deficiency enhances cell-intrinsic ...
Jan 23, 2025 · This basal 'antiviral state' restricts the growth of influenza A virus and is governed by the interaction between proteotoxic stress response ...
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Generation of Human CRY1 and CRY2 Knockout Cells ... - Frontiers
We identified six and two clones (i.e., about 11% of screened clones) with putative deletions in exons corresponding to each of the two alleles of CRY1 and CRY2 ...
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The cry-DASH cryptochrome encoded by the sll1629 gene in the ...
The cry-DASH cryptochrome encoded by the sll1629 gene in the cyanobacterium Synechocystis PCC 6803 is required for Photosystem II repair · 1. Introduction · 2.
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Structure of the bifunctional cryptochrome aCRY from ...
Jul 19, 2018 · The green alga Chlamydomonas reinhardtii harbors one aCRY ortholog (CraCRY) and a plant CRY besides two DASH-type cryptochromes (4,5).
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More Than a Repair Enzyme: Aspergillus nidulans Photolyase-like ...
Cryptochrome-Mediated Light Responses in Plants ... conF and conJ contribute to conidia germination and stress response in the filamentous fungus Aspergillus ...
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Regulation of Conidiation by Light in Aspergillus nidulans - PMC
The activation of these genes may trigger the changes in development, stress responses, and secondary metabolism that A. nidulans undergoes when living in the ...
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Role of Photolyase in Stress Tolerance and Virulence of Plant ...
May 14, 2025 · The cryptochrome ... Role of Photolyase in Stress Tolerance and Virulence of Plant-Pathogenic Bacterium Pseudomonas Cichorii Jbc1.
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European Robin Cryptochrome-4a Associates with Lipid Bilayers in an Ordered Manner, Fulfilling a Molecular-Level Condition for Radical-Pair-Based Magnetoreception
2024 peer-reviewed study in Cells journal on the interaction of European robin CRY4a with lipid bilayers, supporting its potential role in the radical-pair mechanism for avian magnetoreception.