HOXA10-HOXA9

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HOXA10-HOXA9 readthrough is a gene that is unlikely to produce a protein product. [1]

Gene basic physical and functional unit of heredity

In biology, a gene is a sequence of nucleotides in DNA or RNA that codes for a molecule that has a function. During gene expression, the DNA is first copied into RNA. The RNA can be directly functional or be the intermediate template for a protein that performs a function. The transmission of genes to an organism's offspring is the basis of the inheritance of phenotypic trait. These genes make up different DNA sequences called genotypes. Genotypes along with environmental and developmental factors determine what the phenotypes will be. Most biological traits are under the influence of polygenes as well as gene–environment interactions. Some genetic traits are instantly visible, such as eye color or number of limbs, and some are not, such as blood type, risk for specific diseases, or the thousands of basic biochemical processes that constitute life.

Function

This locus represents naturally occurring read-through transcription between the neighboring HOXA10 (homeobox A10) and HOXA9 (full description written out) genes on chromosome 7. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Mar 2011].

Related Research Articles

In the genetic code, a stop codon is a nucleotide triplet within messenger RNA that signals a termination of translation into proteins. Proteins are based on polypeptides, which are unique sequences of amino acids. Most codons in messenger RNA correspond to the addition of an amino acid to a growing polypeptide chain, which may ultimately become a protein. Stop codons signal the termination of this process by binding release factors, which cause the ribosomal subunits to disassociate, releasing the amino acid chain. While start codons need nearby sequences or initiation factors to start translation, a stop codon alone is sufficient to initiate termination.

Pseudogene functionless relative of a gene

Pseudogenes, sometimes referred to as zombie genes in the media, are segments of DNA that are related to real genes. Pseudogenes have lost at least some functionality, relative to the complete gene, in cellular gene expression or protein-coding ability. Pseudogenes often result from the accumulation of multiple mutations within a gene whose product is not required for the survival of the organism, but can also be caused by genomic copy number variation (CNV) where segments of 1+ kb are duplicated or deleted. Although not fully functional, pseudogenes may be functional, similar to other kinds of noncoding DNA, which can perform regulatory functions. The "pseudo" in "pseudogene" implies a variation in sequence relative to the parent coding gene, but does not necessarily indicate pseudo-function. Despite being non-coding, many pseudogenes have important roles in normal physiology and abnormal pathology.

NUP98 protein-coding gene in the species Homo sapiens

Nuclear pore complex protein Nup98-Nup96 is a protein that in humans is encoded by the NUP98 gene.

HOXA9 protein-coding gene in the species Homo sapiens

Homeobox protein Hox-A9 is a protein that in humans is encoded by the HOXA9 gene.

Homeobox A10 protein-coding gene in the species Homo sapiens

Homeobox protein Hox-A10 is a protein that in humans is encoded by the HOXA10 gene.

Homeobox A1 protein-coding gene in the species Homo sapiens

Homeobox protein Hox-A1 is a protein that in humans is encoded by the HOXA1 gene.

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Homeobox protein Meis1 is a protein that in humans is encoded by the MEIS1 gene.

HOXA5 protein-coding gene in the species Homo sapiens

Homeobox protein Hox-A5 is a protein that in humans is encoded by the HOXA5 gene.

HOXA11 protein-coding gene in the species Homo sapiens

Homeobox protein Hox-A11 is a protein that in humans is encoded by the HOXA11 gene.

HOXA7 protein-coding gene in the species Homo sapiens

Homeobox protein Hox-A7 is a protein that in humans is encoded by the HOXA7 gene.

HOXA13 protein-coding gene in the species Homo sapiens

Homeobox protein Hox-A13 is a protein that in humans is encoded by the HOXA13 gene.

PBX2 protein-coding gene in the species Homo sapiens

Pre-B-cell leukemia transcription factor 2 is a protein that in humans is encoded by the PBX2 gene.

HOXA3 protein-coding gene in the species Homo sapiens

Homeobox protein Hox-A3 is a protein that in humans is encoded by the HOXA3 gene.

MEIS2 protein-coding gene in the species Homo sapiens

Homeobox protein Meis2 is a protein that in humans is encoded by the MEIS2 gene.

Gag/pol translational readthrough site

Gag/pol translational readthrough site is a cis-regulatory element found in retroviruses. The readthrough site facilitates the mechanism of translation readthrough of the stop codon at the gag-pol junction producing the gag and pol fusion protein in certain retroviruses. Retroviruses whose gag and pol genes are in the same reading frame often depend upon approximately 5% read-through of the gag UAG termination codon to form the gag-pol polyprotein. This readthrough is usually dependent on a pseudoknot located eight nucleotides downstream of the stop codon (UAG). Sequence conservation is found in the second pseudoknot loop.

Pol refers to a gene in retroviruses, or the protein produced by that gene.

COMMD3-BMI1 protein-coding gene in the species Homo sapiens

The COMMD3-BMI1 gene in humans encodes the COMMD3-BMI1 readthrough protein.

FAM47E-STBD1 protein-coding gene in the species Homo sapiens

FAM47E-STBD1 readthrough is a protein that in humans is encoded by the FAM47E-STBD1 gene.

RNF103-CHMP3 readthrough protein-coding gene in the species Homo sapiens

RNF103-CHMP3 readthrough is a protein that in humans is encoded by the RNF103-CHMP3 gene.

RAB4B-EGLN2 readthrough is a protein that in humans is encoded by the RAB4B-EGLN2 gene.

References

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

United States National Library of Medicine the worlds largest medical library, operated by the US federal government

The United States National Library of Medicine (NLM), operated by the United States federal government, is the world's largest medical library.

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