Nuclear protein in testis gene: Difference between revisions

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{{PAGENAME}} - human nutm1 wild type allele is located in the vicinity of 15q14 and is approximately 14 kb in length. This allele, which encodes nut family member 1 protein, may play a role in the function of the testes. A chromosomal aberration t(15;19)(q13;p13.1) involving the gene and the human brd4 gene is associated with a lethal midline thoracic, head and neck carcinoma.
{{DISPLAYTITLE:Nuclear protein in testis gene}}
{{med-stub}}
{{Infobox gene
{{dictionary-stub2}}
| name = Nuclear protein in testis
| symbol = NUT
| HGNCid = 8060
| chromosome = 15
| arm = q
| band = 14
}}
 
The '''Nuclear protein in testis''' ('''NUT''') gene is a [[gene]] that encodes a protein primarily expressed in the [[testis]]. It is located on the long arm of [[chromosome 15]] at band q14. The NUT gene is of significant interest in medical research due to its involvement in certain [[cancer]]s, particularly [[NUT midline carcinoma]].
 
==Structure==
The NUT gene is composed of several [[exons]] and [[introns]], which are transcribed into [[mRNA]] and subsequently translated into the NUT protein. The protein itself is characterized by its nuclear localization, indicating its role in the [[nucleus]] of the cell. The exact structure of the NUT protein includes domains that are involved in [[chromatin]] binding and [[transcriptional regulation]].
 
==Function==
The primary function of the NUT protein is not fully understood, but it is believed to play a role in [[chromatin remodeling]] and [[gene expression]] regulation. Its expression is normally restricted to the testis, suggesting a role in [[spermatogenesis]] or other testis-specific functions.
 
==Pathology==
===NUT Midline Carcinoma===
NUT midline carcinoma (NMC) is a rare and aggressive form of cancer that is characterized by the presence of a chromosomal translocation involving the NUT gene. The most common translocation is t(15;19)(q14;p13.1), which results in the fusion of the NUT gene with the [[BRD4]] gene. This fusion protein is oncogenic and leads to the development of NMC, which typically occurs in the midline structures of the body, such as the [[mediastinum]] and [[head and neck]] region.
 
===Diagnosis===
Diagnosis of NUT midline carcinoma is confirmed through [[cytogenetic]] analysis or [[fluorescence in situ hybridization]] (FISH) to detect the NUT gene rearrangement. [[Immunohistochemistry]] can also be used to identify the presence of the NUT protein in tumor samples.
 
===Treatment===
Treatment options for NUT midline carcinoma are limited and often involve a combination of [[surgery]], [[chemotherapy]], and [[radiation therapy]]. Recent research has focused on targeted therapies that inhibit the function of the BRD4-NUT fusion protein, such as [[bromodomain]] inhibitors.
 
==Research Directions==
Ongoing research is aimed at better understanding the normal function of the NUT protein in testis and its role in oncogenesis. Studies are also exploring novel therapeutic approaches to target NUT midline carcinoma more effectively.
 
==See Also==
* [[Chromatin remodeling]]
* [[Gene expression]]
* [[Oncogene]]
* [[Testis]]
 
==External Links==
* [NUT gene at HGNC](https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/8060)
* [NUT midline carcinoma information at NCI](https://www.cancer.gov/types/nut-midline-carcinoma)
 
{{Genetics-stub}}
{{Cancer-stub}}
 
[[Category:Genes on human chromosome 15]]
[[Category:Oncogenes]]
[[Category:Testis-specific genes]]

Latest revision as of 21:43, 1 January 2025


Nuclear protein in testis
Symbol NUT
HGNC ID 8060
Alternative symbols
Entrez Gene
OMIM
RefSeq
UniProt
Chromosome 15q14
Locus supplementary data


The Nuclear protein in testis (NUT) gene is a gene that encodes a protein primarily expressed in the testis. It is located on the long arm of chromosome 15 at band q14. The NUT gene is of significant interest in medical research due to its involvement in certain cancers, particularly NUT midline carcinoma.

Structure[edit]

The NUT gene is composed of several exons and introns, which are transcribed into mRNA and subsequently translated into the NUT protein. The protein itself is characterized by its nuclear localization, indicating its role in the nucleus of the cell. The exact structure of the NUT protein includes domains that are involved in chromatin binding and transcriptional regulation.

Function[edit]

The primary function of the NUT protein is not fully understood, but it is believed to play a role in chromatin remodeling and gene expression regulation. Its expression is normally restricted to the testis, suggesting a role in spermatogenesis or other testis-specific functions.

Pathology[edit]

NUT Midline Carcinoma[edit]

NUT midline carcinoma (NMC) is a rare and aggressive form of cancer that is characterized by the presence of a chromosomal translocation involving the NUT gene. The most common translocation is t(15;19)(q14;p13.1), which results in the fusion of the NUT gene with the BRD4 gene. This fusion protein is oncogenic and leads to the development of NMC, which typically occurs in the midline structures of the body, such as the mediastinum and head and neck region.

Diagnosis[edit]

Diagnosis of NUT midline carcinoma is confirmed through cytogenetic analysis or fluorescence in situ hybridization (FISH) to detect the NUT gene rearrangement. Immunohistochemistry can also be used to identify the presence of the NUT protein in tumor samples.

Treatment[edit]

Treatment options for NUT midline carcinoma are limited and often involve a combination of surgery, chemotherapy, and radiation therapy. Recent research has focused on targeted therapies that inhibit the function of the BRD4-NUT fusion protein, such as bromodomain inhibitors.

Research Directions[edit]

Ongoing research is aimed at better understanding the normal function of the NUT protein in testis and its role in oncogenesis. Studies are also exploring novel therapeutic approaches to target NUT midline carcinoma more effectively.

See Also[edit]

External Links[edit]

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