Target Name: MEIS2
NCBI ID: G4212
Other Name(s): Meis homeobox 2, transcript variant c | TALE homeobox protein Meis2 | Homeobox protein Meis2 (isoform f) | HsT18361 | Meis1-related gene 1 | MEIS2_HUMAN | Meis homeobox 2, transcript variant b | Meis (mouse) homolog 2 | Meis homeobox 2, transcript variant g | Homeobox protein Meis2 (isoform c) | Meis1, myeloid ecotropic viral integration site 1 homolog 2 | Homeobox protein Meis2 (isoform b) | MEIS2 variant a | MRG1 | Meis homeobox 2 | Meis homeobox 2, transcript variant f | Homeobox protein Meis2 (isoform a) | MEIS2 variant c | Homeobox protein Meis2 | MEIS2 variant g | Meis homeobox 2, transcript variant a | MEIS2 variant b | MGC2820 | Meis1-related protein 1 | MEIS2 variant f | Meis homolog 2 | CPCMR | meis1-related protein 1 | Homeobox protein Meis2 (isoform g)

Targeting MEIS2: Developing Drugs for Nervous System Disorders

MEIS2 (Meis homeobox 2) is a gene that encodes a protein known as Meis2, which is a key component of the homeobox gene family. Homeobox genes are a family of genes that are responsible for the development and maintenance of various body systems, including the nervous system. MEIS2 is a member of this family and is involved in the development and maintenance of the nervous system.

Disease and Abnormalities

MEIS2 is involved in a number of normal processes in the nervous system, but it is also implicated in a number of diseases and abnormalities. One of the main functions of MEIS2 is to help regulate the development and organization of the nervous system during embryonic development. This is important for the development and function of the nervous system, and is critical for the development of healthy individuals.

However, when MEIS2 is disrupted or expressed at high levels, it can cause a number of different diseases and abnormalities. For example, MEIS2 is often expressed in individuals with Down syndrome, a genetic disorder that affects the development of the nervous system. In these individuals, high levels of MEIS2 can lead to the development of neuronal abnormalities, including an overgrowth of neurons and an imbalance of different types of neurons. This can lead to a range of symptoms, including cognitive and motor impairments.

Another example of a disease that is associated with MEIS2 is the development of leukemia.MEIS2 has been shown to be highly expressed in various types of leukemia, and high levels of MEIS2 have been linked to the development of these diseases.

Furthermore,MEIS2 is also involved in the development and progression of neurodegenerative diseases, such as Alzheimer's disease and Parkinson's disease.MEIS2 has been shown to be expressed in the brains of individuals with these conditions, and high levels of MEIS2 have been linked to the development and progression of these diseases.

Drugs and Treatments

Given the involvement of MEIS2 in a number of diseases and abnormalities, researchers have been interested in developing drugs and treatments that can target this gene. Currently, there are several drugs that are being developed to target MEIS2, including gene therapies and small molecules that can inhibit the activity of MEIS2.

One of the most promising avenues for targeting MEIS2 is the use of gene therapies. Gene therapies are a type of therapy that uses genes to treat or prevent diseases. By using genes that are naturally present in the body, gene therapies can avoid the potential side effects of traditional medications. Currently, researchers are working on developing gene therapies that can target MEIS2 and correct its abnormal functions.

Another approach to targeting MEIS2 is the use of small molecules that can inhibit the activity of MEIS2. These small molecules, called inhibitors, can be used to treat diseases associated with high levels of MEIS2, such as Down syndrome, leukemia, and neurodegenerative diseases.

Conclusion

MEIS2 is a gene that is involved in the development and maintenance of the nervous system. It is often expressed at high levels in individuals with Down syndrome and other diseases, and is linked to a number of different abnormalities. As a result, researchers are interested in developing drugs and treatments that can target MEIS2 and correct its abnormal functions. With the development of gene therapies and small molecules that can inhibit the activity of MEIS2, there is hope for the development of new treatments for a number of diseases associated with high levels of MEIS2.

Protein Name: Meis Homeobox 2

Functions: Involved in transcriptional regulation. Binds to HOX or PBX proteins to form dimers, or to a DNA-bound dimer of PBX and HOX proteins and thought to have a role in stabilization of the homeoprotein-DNA complex. Isoform 3 is required for the activity of a PDX1:PBX1b:MEIS2b complex in pancreatic acinar cells involved in the transcriptional activation of the ELA1 enhancer; the complex binds to the enhancer B element and cooperates with the transcription factor 1 complex (PTF1) bound to the enhancer A element; MEIS2 is not involved in complex DNA-binding. Probably in complex with PBX1, is involved in transcriptional regulation by KLF4. Isoform 3 and isoform 4 can bind to a EPHA8 promoter sequence containing the DNA motif 5'-CGGTCA-3'; in cooperation with a PBX protein (such as PBX2) is proposed to be involved in the transcriptional activation of EPHA8 in the developing midbrain. May be involved in regulation of myeloid differentiation. Can bind to the DNA sequence 5'-TGACAG-3'in the activator ACT sequence of the D(1A) dopamine receptor (DRD1) promoter and activate DRD1 transcription; isoform 5 cannot activate DRD1 transcription

More Common Targets

MEIS3 | MEIS3P1 | MEIS3P2 | Melanin | Melanin-concentrating hormone (MCH) receptor | Melanocortin receptor | Melanoma-Associated Antigen | Melatonin receptor | MELK | MELTF | MELTF-AS1 | Membrane-Bound Protein Tyrosine Phosphatases (rPTPs) | Membrane-spanning 4-domains subfamily A member 4A | MEMO1 | MEMO1P1 | MEMO1P4 | MEMO1P5 | MEN1 | MEOX1 | MEOX2 | MEP1A | MEP1AP2 | MEP1AP4 | MEP1B | MEPCE | MEPE | MERTK | MESD | MESP1 | MESP2 | MEST | MESTIT1 | MESTP3 | MESTP4 | MET | Metabotropic glutamate (mGluR) receptor | Metallothionein | METAP1 | METAP1D | METAP2 | Metaxin complex | Methionine adenosyltransferase | Methionine adenosyltransferase II | Methionyl aminopeptidase | Methylcytosine dioxygenase (TET) | METRN | METRNL | METTL1 | METTL13 | METTL14 | METTL15 | METTL15P1 | METTL15P2 | METTL16 | METTL17 | METTL18 | METTL21A | METTL21C | METTL21EP | METTL22 | METTL23 | METTL24 | METTL25 | METTL25B | METTL26 | METTL27 | METTL2A | METTL2B | METTL3 | METTL4 | METTL5 | METTL6 | METTL7A | METTL7B | METTL8 | METTL9 | MEX3A | MEX3B | MEX3C | MEX3D | MFAP1 | MFAP2 | MFAP3 | MFAP3L | MFAP4 | MFAP5 | MFF | MFF-DT | MFGE8 | MFHAS1 | MFN1 | MFN2 | MFNG | MFRP | MFSD1 | MFSD10 | MFSD11 | MFSD12 | MFSD13A | MFSD14A