60S ribosomal protein L41

60S ribosomal protein L41 is a protein that is specific to humans and is encoded by the RPL41 gene,[3][4][5] also known as HG12 and large eukaryotic ribosomal subunit protein eL41.[6]  The gene family HGNC is L ribosomal proteins. The protein itself is also described as P62945-RL41_HUMAN on the GeneCards database.[7] This RPL41 gene is located on chromosome 12.[6]

RPL41
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesRPL41, L41, ribosomal protein L41
External IDsOMIM: 613315 GeneCards: RPL41
Orthologs
SpeciesHumanMouse
Entrez

6171

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Ensembl

ENSG00000229117

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UniProt

P62945

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RefSeq (mRNA)

NM_021104
NM_001035267

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RefSeq (protein)

NP_001030344
NP_066927

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Location (UCSC)Chr 12: 56.12 – 56.12 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. The 60S subunit is a chain of only 25 amino acids and contains an alpha helix and a turn. This is significantly smaller than most ribosomal sequences of around 80 amino acids. The alpha helix is from amino acid three to fourteen, and the turn is from position fifteen to eighteen.[6] Of these 25 amino acids, most of them are arginine or lysine.[8] This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein, which shares sequence similarity with the yeast ribosomal protein YL41, belongs to the L41E family of ribosomal proteins. It is located in the cytoplasm. The gene is made up of three introns in between four exons. Exon 1 is 36 nucleotides long, exon 2 is 25 nucleotides long, exon 3 is 23 nt, and exon 4 is 346 nt. Intron 1 is 115 nucleotides, intron 2 is 389 nt, and intron 3 is 275 nt. Differently from the yeast gene, the introns were only observed in the human gene, although the exons were 99.5% homologous.[9]

Gene expression

The protein is found in six tissues: the immune, nervous, muscle, internal, secretory, and reproductive systems. There are 37 major tissues included in the chart by GeneCards.[7] Overall, the gene expression for the major tissues of these six systems is highest in RNA sequencing with expression seen in 32 out of 37 major tissues . The least amount of gene expression seen is in the Serial Analysis of Gene Expression (SAGE) with expression seen in 20 out of 37 tissues. The medium amount of RPL41 expression was 27 out of 37 tissues in Microarray.[7]

In the immune system, the protein is expressed in the whole blood cells, white blood cells, and lymph nodes of RNA sequencing. The protein is expressed for Serial Analysis of Gene Expression (SAGE) in the bone marrow and lymph nodes. Microarray shows expression for the protein in bone marrow, whole blood cells, lymph nodes, and the thymus. The only major tissue of the immune system with expression measured for all three categories; RNA sequencing, Microarray, SAGE, is in the lymph nodes.[7]

In the nervous system, the protein is expressed in the brain, cortex, cerebellum, spinal cord, and tibial nerve of RNA sequencing. These tissues also express the protein, excluding the tibial nerve and including the retina. Microarray shows expression for the protein in the brain, cerebellum, retina, and spinal cord.[7]

In the muscle system, both the heart and skeletal muscle show expression for the RPL41 gene in RNA sequencing, Microarray, and SAGE. Expression in the arteries for the protein is only shown in RNA sequencing. The smooth muscle only shows expression of the protein in Microarray.[7]

There is expression of the gene in all major tissues of the internal system for RNA sequencing; small intestine, colon, adipocyte, kidney, liver, lung, spleen, stomach, esophagus, and bladder. In the Microarray, gene expression is found in the small intestine, colon, adipocyte, kidney, liver, and lungs. In SAGE, there is gene expression in the colon, kidney, liver, and lung.[7]

There is expression of the gene in all major tissues of the secretory system for RNA sequencing; pancreas, thyroid, salivary gland, adrenal gland, pituitary, breast, and skin. In the Microarray, gene expression is found in the pancreas, thyroid, salivary gland, adrenal gland, and skin. In SAGE, there is gene expression in the pancreas, thyroid, breast, and skin.[7]

There is expression of the gene in all major tissues of the reproductive system for Microarray; ovary, uterus, placenta, prostate, and testes. In RNA sequencing, gene expression is found in the ovary, uterus, prostate, and testes. In SAGE, there is only gene expression in the placenta and testes.[7]

Comparison between species

Similar to the 60S ribosomal protein L41, the PsRbL41 in pea root caps has almost the same chain of amino acids. These are also closely related to 60S ribosomal protein YL41 in yeast and cotton. This PsRbL41 protein acts with PsHRGP1 and PsCaP23 in the process of cell reproduction.[10] Yuen-Ling Chan, Joe Olvera, and Ira G. Wool compared the human 60S ribosomal subunit L41 to the same DNA sequence in rats. The ribosomal proteins L4 and L41 in rats were isolated and replicated to analyze the sequences. Overall, the sequences were 93% identical between rat and human. The beginning of the sequences had a closer match of 97% than compared to the end of the sequence of 75%. This difference also occurred in comparisons with other species, with 92% and 39% of Xenopus laevis L1a and L1b.[11]

Function

The protein can interact with the beta subunit of protein kinase CKII and can stimulate the phosphorylation of DNA topoisomerase II-alpha by CKII. The main functions are to enable mRNA 3’-UTR binding and make up the structure of the ribosome. It is also a part of peptide chain elongation and processes rRNA in the nucleus and cytosol.[7] In yeast, the length of the UTRs are varied from other genes, with 18-22 nucleotides at the 5’ side and 203-210 on the 3’ side. The estimated time for translation of the L41 ribosome was calculated to be approximately 2 seconds in a study by Xiang Yu and Jonathan R. Warner.[12] In the Variant viewer of the UniProt 60S ribosomal protein L41, 15 possible variants are shown from the amino acids in position 3 to 20. These changes are all by missense mutations of base substitution, except for one nonsense mutation with a stop codon added. The chart shows 14 of the variants as predicted to have a consequence and 1 variant uncertain.[6] The most common amino acid change is from G to A and G to T. Other mutations observed were G to C, C to A, and A to C. There are no observed frameshift mutations of deletion or insertion, only amino acid changes. There is also no methylation seen in the interactions of the 60S ribosomal protein subunit L41. There is no drug resistance found for the mutations described. [13] Although the gene is typically expressed, the deletion of the ribosomal protein L41 in yeast does not prevent the growth of the organism.[12] Two alternative splice variants have been identified, both encoding the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome.[5]

References

  1. GRCh38: Ensembl release 89: ENSG00000229117 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. Klaudiny J, von der Kammer H, Scheit KH (September 1992). "Characterization by cDNA cloning of the mRNA of a highly basic human protein homologous to the yeast ribosomal protein YL41". Biochemical and Biophysical Research Communications. 187 (2): 901–906. doi:10.1016/0006-291X(92)91282-U. PMID 1326959.
  4. Kenmochi N, Kawaguchi T, Rozen S, Davis E, Goodman N, Hudson TJ, et al. (May 1998). "A map of 75 human ribosomal protein genes". Genome Research. 8 (5): 509–523. doi:10.1101/gr.8.5.509. PMID 9582194.
  5. "RPL41 ribosomal protein L41". Entrez Gene. U.S. National Library of Medicine.
  6. "RL41_HUMAN". UniProt. P62945. Retrieved 2023-05-02.
  7. "RPL41". GeneCards.
  8. "Ribosomal protein L41". InterPro. IPR007836.
  9. Go H, Miyado K, Taniguchi S (December 1998). "Genomic structure of the human ribosomal protein L41 gene". Biochemistry and Molecular Biology International. 46 (6): 1227–1231. doi:10.1080/15216549800204792. PMID 9891856.
  10. Woo HH, Hawes MC (December 1997). "Cloning of genes whose expression is correlated with mitosis and localized in dividing cells in root caps of Pisum sativum L". Plant Molecular Biology. 35 (6): 1045–1051. doi:10.1023/a:1005930625920. PMID 9426627.
  11. Chan YL, Olvera J, Wool IG (September 1995). "The primary structures of rat ribosomal proteins L4 and L41". Biochemical and Biophysical Research Communications. 214 (3): 810–818. doi:10.1006/bbrc.1995.2359. PMID 7575549.
  12. Yu X, Warner JR (September 2001). "Expression of a micro-protein". The Journal of Biological Chemistry. 276 (36): 33821–33825. doi:10.1074/jbc.M103772200. PMID 11451953.
  13. "RPL41 Gene View". Catalogue of Somatic Mutations in Cancer.

Further reading

  • Wool IG, Chan YL, Glück A (1996). "Structure and evolution of mammalian ribosomal proteins". Biochemistry and Cell Biology. 73 (11–12): 933–947. doi:10.1139/o95-101. PMID 8722009.
  • Kato S, Sekine S, Oh SW, Kim NS, Umezawa Y, Abe N, et al. (December 1994). "Construction of a human full-length cDNA bank". Gene. 150 (2): 243–250. doi:10.1016/0378-1119(94)90433-2. PMID 7821789.
  • Lee JH, Kim JM, Kim MS, Lee YT, Marshak DR, Bae YS (September 1997). "The highly basic ribosomal protein L41 interacts with the beta subunit of protein kinase CKII and stimulates phosphorylation of DNA topoisomerase IIalpha by CKII". Biochemical and Biophysical Research Communications. 238 (2): 462–467. doi:10.1006/bbrc.1997.7317. PMID 9299532.
  • Go H, Miyado K, Taniguchi S (December 1998). "Genomic structure of the human ribosomal protein L41 gene". Biochemistry and Molecular Biology International. 46 (6): 1227–1231. doi:10.1080/15216549800204792. PMID 9891856. S2CID 6514753.
  • Uechi T, Tanaka T, Kenmochi N (March 2001). "A complete map of the human ribosomal protein genes: assignment of 80 genes to the cytogenetic map and implications for human disorders". Genomics. 72 (3): 223–230. doi:10.1006/geno.2000.6470. PMID 11401437.
  • Ahn BH, Kim TH, Bae YS (October 2001). "Mapping of the interaction domain of the protein kinase CKII beta subunit with target proteins". Molecules and Cells. 12 (2): 158–163. PMID 11710515.
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