Difference between revisions of "NONHSAT035776"
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==Annotated Information==
===Transcriptomic Nomeclature===
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[[Category:Intergenic]] | [[Category:Intergenic]] | ||
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+ | {{lncrnadb| | ||
+ | tID = NONHSAT035776| | ||
+ | ltID = TEA ncRNAs| | ||
+ | ann = <tab class=wikitable sep=tab head=top> | ||
+ | Section Description | ||
+ | ID TEA ncRNAs | ||
+ | Characteristics TEA ncRNAs transcripts originate from the TEA ncRNAs promoter at the 5' of the array of joining (J) gene segments of the T-cell receptor alpha chain (TCRA) [http://www.ncbi.nlm.nih.gov/pubmed/3500476 (de Villartay (1987))]. Another noncoding transcript has been identified coming from a promoter within the J array (J-alpha 49).<br /> TEA ncRNAs transcription extends up to ~71kb, covering the length of the J array and terminating in the C alpha region [http://www.ncbi.nlm.nih.gov/pubmed/3500476 (de Villartay (1987))]. . Full length of actual spliced TEA ncRNAs transcript reported as ~2kb [http://www.ncbi.nlm.nih.gov/pubmed/3500476 (de Villartay (1987)], [http://www.ncbi.nlm.nih.gov/pubmed/8383995 Shimizu (1993)]). ~4.5 and 8kb transcripts have also been reported. Transcripts generally include TEA ncRNAs sequence spliced to C alpha and sometimes include J segments [http://www.ncbi.nlm.nih.gov/pubmed/9247569 (Villey (1997))]. | ||
+ | Expression Expressed during thymocyte development at a time recombination is occurring ([http://www.ncbi.nlm.nih.gov/pubmed/16936730 Abarrategui (2006)], [http://www.ncbi.nlm.nih.gov/pubmed/17882258 Abarrategui (2007)]). Expression is highest in fetal thymocytes and is absent in mature adult T cells ([http://www.ncbi.nlm.nih.gov/pubmed/3500476 de Villartay (1987)], [http://www.ncbi.nlm.nih.gov/pubmed/8383995 Shimizu (1993)]).<br /> TEA ncRNAs transcripts have been identified in the nucleus [http://www.ncbi.nlm.nih.gov/pubmed/17882258 (Abarrategui (2007))]. | ||
+ | Function TEA ncRNAs transcription regulates V alpha-to-J alpha recombination and is necessary to generate the full complement of recombined segments ([http://www.ncbi.nlm.nih.gov/pubmed/16936730 Abarrategui (2006)], [http://www.ncbi.nlm.nih.gov/pubmed/17882258 Abarrategui (2007)]).<br /> Transcription has both activating and repressive effects on the promoters of different J segments. Segments only a small distance downstream from the TEA ncRNAs promoter are activated while segments more distal are repressed, with alterations in histone modifications and chromatin accessibility ([http://www.ncbi.nlm.nih.gov/pubmed/16936730 Abarrategui (2006)], [http://www.ncbi.nlm.nih.gov/pubmed/17882258 Abarrategui (2007)]).<br /> These effects target initial recombination events to the active proximal J segments. In the absence of TEA ncRNAs ncRNA transcription recombination occurs in more distal J segments which are normally repressed ([http://www.ncbi.nlm.nih.gov/pubmed/16936730 Abarrategui (2006)], [http://www.ncbi.nlm.nih.gov/pubmed/17882258 Abarrategui (2007)]).<br /> Repressive effects of the TEA ncRNAs ncRNA suggested to be due to transcriptional interference. Unknown if TEA ncRNAs ncRNA also has a function itself, ie: recruitment of chromatin modification complexes ([http://www.ncbi.nlm.nih.gov/pubmed/16936730 Abarrategui (2006)], [http://www.ncbi.nlm.nih.gov/pubmed/17882258 Abarrategui (2007)]). | ||
+ | Conservation Humans and mouse ([http://www.ncbi.nlm.nih.gov/pubmed/3500476 de Villartay (1987)], [http://www.ncbi.nlm.nih.gov/pubmed/8383995 Shimizu (1993)]). | ||
+ | Misc V(D)J recombination acts to assemble the variable regions of T cell receptors from germline variable (V), diversity (D) and joining (J) gene segments.<br /> RNA accessions from [http://www.ncbi.nlm.nih.gov/pubmed/3500476 de Villartay (1987)] and [http://www.ncbi.nlm.nih.gov/pubmed/8383995 Shimizu (1993)] some are spliced some are not.<br /> Human 147: GenBank: M18204.1. Human 147A1: GenBank: M18206.1. Human 147A19: GenBank: M18205.1. Mouse T early alpha (TEA ncRNAs) region: GenBank: D13547.1 | ||
+ | Name TEA ncRNAs: T early alpha | ||
+ | </tab>| | ||
+ | }} |
Revision as of 12:20, 6 October 2014
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Contents
Annotated Information
Transcriptomic Nomeclature
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Function
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Regulation
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Expression
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Allelic Information and Variation
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Evolution
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You can also add sub-section(s) at will.
Labs working on this lncRNA
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References
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Basic Information
Transcript ID |
NONHSAT035776 |
Source |
NONCODE4.0 |
Same with |
, |
Classification |
intergenic |
Length |
506 nt |
Genomic location |
chr14+:22942568..23016567 |
Exon number |
2 |
Exons |
22942568..22942930,23016447..23016567 |
Genome context |
|
Sequence |
000001 GAATTCATGT CTTACGGTCA AGGGCTAGAG AAAGGATTTC TGCATCACTT TCTTCCTGTA GCAATTCCAT CCGAGATCCC 000080
000081 TGGGACAGAC CTGGCCTGAT GAATAGCAGG AAGCACACCA GGGAGGGACA AGGTCCTGCA GACAACCTTC ACCACCAGGC 000160 000161 TGGGACAGCG CCATGGGGAC CCAGGGCCTC TGCTTTGGGG AAAGACCTTG CTGAGGGGCC CCATGGGCAA GAACAAGTGT 000240 000241 GAAGAACCCT ACTATGGTTT TTTGCCCAAT GCCCTCCACA AAGCCAGCGT TTGAAGGAAA ACTGTGAGGA AGAAGGGACA 000320 000321 CTCCATGGTG TTGTTGTTGC CACCTCTGGA GCAGCCTGTA GCAAGAACAG TCTTGGTCCA ACCAGATATC CAGAAGCCTG 000400 000401 ACCCTGCCGT GTACCAGCTG AGAGACTCTA AATCCAGTGA CAAGTCTGTC TGCCTATTCA CCGATTTTGA TTCTCAAACA 000480 000481 AATGTGTCAC AAAGTAAGGA TTCTGA |
Annotation (From lncRNAdb)
Section | Description |
---|---|
ID | TEA ncRNAs |
Characteristics | TEA ncRNAs transcripts originate from the TEA ncRNAs promoter at the 5' of the array of joining (J) gene segments of the T-cell receptor alpha chain (TCRA) (de Villartay (1987)). Another noncoding transcript has been identified coming from a promoter within the J array (J-alpha 49). TEA ncRNAs transcription extends up to ~71kb, covering the length of the J array and terminating in the C alpha region (de Villartay (1987)). . Full length of actual spliced TEA ncRNAs transcript reported as ~2kb (de Villartay (1987), Shimizu (1993)). ~4.5 and 8kb transcripts have also been reported. Transcripts generally include TEA ncRNAs sequence spliced to C alpha and sometimes include J segments (Villey (1997)). |
Expression | Expressed during thymocyte development at a time recombination is occurring (Abarrategui (2006), Abarrategui (2007)). Expression is highest in fetal thymocytes and is absent in mature adult T cells (de Villartay (1987), Shimizu (1993)). TEA ncRNAs transcripts have been identified in the nucleus (Abarrategui (2007)). |
Function | TEA ncRNAs transcription regulates V alpha-to-J alpha recombination and is necessary to generate the full complement of recombined segments (Abarrategui (2006), Abarrategui (2007)). Transcription has both activating and repressive effects on the promoters of different J segments. Segments only a small distance downstream from the TEA ncRNAs promoter are activated while segments more distal are repressed, with alterations in histone modifications and chromatin accessibility (Abarrategui (2006), Abarrategui (2007)). These effects target initial recombination events to the active proximal J segments. In the absence of TEA ncRNAs ncRNA transcription recombination occurs in more distal J segments which are normally repressed (Abarrategui (2006), Abarrategui (2007)). Repressive effects of the TEA ncRNAs ncRNA suggested to be due to transcriptional interference. Unknown if TEA ncRNAs ncRNA also has a function itself, ie: recruitment of chromatin modification complexes (Abarrategui (2006), Abarrategui (2007)). |
Conservation | Humans and mouse (de Villartay (1987), Shimizu (1993)). |
Misc | V(D)J recombination acts to assemble the variable regions of T cell receptors from germline variable (V), diversity (D) and joining (J) gene segments. RNA accessions from de Villartay (1987) and Shimizu (1993) some are spliced some are not. Human 147: GenBank: M18204.1. Human 147A1: GenBank: M18206.1. Human 147A19: GenBank: M18205.1. Mouse T early alpha (TEA ncRNAs) region: GenBank: D13547.1 |
Name | TEA ncRNAs: T early alpha |