The protein Dynein Intermediate Chain (Dynein IC) plays a pivotal role in the cellular architecture and function. As part of the cytoplasmic dynein complex, it is integral in the movement of vesicles, organelles, and other cargos along microtubules within the cell. This motor protein is essential for various dynamic processes such as mitosis, where it assists in chromosome alignment and segregation, and in the transport of neurotransmitters within neurons. Dynein IC is also implicated in the positioning of organelles like the Golgi apparatus and lysosomes, facilitating cellular homeostasis and signaling. The regulation of Dynein IC expression is a finely tuned process, influenced by a network of signals that ensure its levels are appropriate for cellular needs. Understanding the regulation of Dynein IC is of fundamental importance in cell biology, as it provides insights into the intricate system of intracellular transport and its coordination with cellular activities.
In the quest to understand the regulation of Dynein IC, various chemical compounds have been identified that can potentially induce its expression. These activators range from naturally occurring substances to synthetic molecules, each interacting with unique cellular pathways to upregulate the synthesis of Dynein IC. For example, signaling molecules like forskolin can raise intracellular cAMP, which might lead to enhanced expression of Dynein IC by activating protein kinase A (PKA) and modulating transcription factors. Epigenetic modulators such as Trichostatin A and 5-Azacytidine can alter the chromatin structure, making the Dynein IC gene more accessible to the transcriptional machinery, thereby promoting its expression. Other natural compounds like resveratrol, found in red grapes, and epigallocatechin gallate, prevalent in green tea, are known activators that can stimulate expression by engaging with cellular antioxidant defenses and metabolic pathways. These activators elucidate the diverse molecular mechanisms through which Dynein IC expression can be regulated, contributing to our understanding of cellular function and the complex regulation of motor proteins.
SEE ALSO...
Items 1 to 10 of 12 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid can upregulate gene transcription via retinoic acid receptors, possibly leading to an increase in Dynein IC synthesis due to enhanced gene activation. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Forskolin stimulates adenylate cyclase, which elevates cAMP levels, potentially initiating a signaling cascade that upregulates the expression of proteins including Dynein IC. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A, as a histone deacetylase inhibitor, promotes chromatin expansion, facilitating the transcriptional machinery's access to DNA, which may stimulate Dynein IC gene expression. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine can lead to the reactivation of silenced genes by DNA demethylation, which could trigger an upsurge in Dynein IC production by removing epigenetic repression. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium chloride inhibits GSK-3 activity, which could initiate a downstream increase in the expression of certain proteins, including Dynein IC, through altered transcriptional control. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
This catechin has been reported to stimulate antioxidant response elements, which could lead to an upregulation of protective cellular proteins, potentially including Dynein IC. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $30.00 $46.00 $82.00 $218.00 | 19 | |
Sodium butyrate, as a histone deacetylase inhibitor, can induce hyperacetylation of histones, thus promoting gene transcription of various proteins, possibly including Dynein IC. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
Resveratrol is suggested to activate sirtuin pathways, which might initiate the transcription of longevity-associated proteins, potentially leading to a surge in Dynein IC levels. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
Curcumin has been reported to stimulate nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), which can lead to the transcriptional activation of multiple genes, including Dynein IC. | ||||||
β-Estradiol | 50-28-2 | sc-204431 sc-204431A | 500 mg 5 g | $62.00 $178.00 | 8 | |
β-Estradiol binds to estrogen receptors and can stimulate the transcription of a range of target genes, which may result in an upregulation of Dynein IC expression. | ||||||