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Identification of a novel nucleolin related protein (NRP) gene expressed during rat spermatogenesis
BACKGROUND: Nucleolin is a major nucleolar phosphoprotein involved in various steps of ribosome biogenesis in eukaryotic cells. As nucleolin plays a significant role in ribosomal RNA transcription we were interested in examining in detail the expression of nucleolin across different stages of sperma...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2711064/ https://www.ncbi.nlm.nih.gov/pubmed/19570216 http://dx.doi.org/10.1186/1471-2199-10-64 |
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author | Chathoth, Keerthi T Ganesan, Gayatri Rao, MRS |
author_facet | Chathoth, Keerthi T Ganesan, Gayatri Rao, MRS |
author_sort | Chathoth, Keerthi T |
collection | PubMed |
description | BACKGROUND: Nucleolin is a major nucleolar phosphoprotein involved in various steps of ribosome biogenesis in eukaryotic cells. As nucleolin plays a significant role in ribosomal RNA transcription we were interested in examining in detail the expression of nucleolin across different stages of spermatogenesis and correlate with the transcription status of ribosomal DNA in germ cells. RESULTS: By RT PCR and western blot analysis we found that nucleolin is strongly down regulated in meiotic spermatocytes and haploid germ cells. We have identified a new nucleolin related protein (NRP) gene in the rat genome, which is over expressed in the testis and is up regulated several fold in meiotic spermatocytes and haploid germ cells. The NRP protein lacks the acidic stretches in its N terminal domain, and it is encoded in rat chromosome 15 having a different genomic organization as compared to nucleolin gene present on chromosome 9. We have also found NRP genes encoded in genomes of other mammalian species. We performed run-on transcription assay where we have observed that rDNA is transcribed at much lower level in meiotic spermatocytes and haploid spermatids as compared to diploid cells. By siRNA knock down experiments we could also demonstrate that NRP can support rDNA transcription in the absence of nucleolin. CONCLUSION: We have identified a new nucleolin variant over expressed in germ cells in rat and analyzed its domain structure. We attribute that the transcriptional activity of rDNA genes in the late spermatogenesis is due to the presence of this variant NRP. The expression of this variant in the germ cells in the absence of nucleolin, could have additional functions in the mammalian spermatogenesis which needs to be investigated further. |
format | Text |
id | pubmed-2711064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27110642009-07-16 Identification of a novel nucleolin related protein (NRP) gene expressed during rat spermatogenesis Chathoth, Keerthi T Ganesan, Gayatri Rao, MRS BMC Mol Biol Research Article BACKGROUND: Nucleolin is a major nucleolar phosphoprotein involved in various steps of ribosome biogenesis in eukaryotic cells. As nucleolin plays a significant role in ribosomal RNA transcription we were interested in examining in detail the expression of nucleolin across different stages of spermatogenesis and correlate with the transcription status of ribosomal DNA in germ cells. RESULTS: By RT PCR and western blot analysis we found that nucleolin is strongly down regulated in meiotic spermatocytes and haploid germ cells. We have identified a new nucleolin related protein (NRP) gene in the rat genome, which is over expressed in the testis and is up regulated several fold in meiotic spermatocytes and haploid germ cells. The NRP protein lacks the acidic stretches in its N terminal domain, and it is encoded in rat chromosome 15 having a different genomic organization as compared to nucleolin gene present on chromosome 9. We have also found NRP genes encoded in genomes of other mammalian species. We performed run-on transcription assay where we have observed that rDNA is transcribed at much lower level in meiotic spermatocytes and haploid spermatids as compared to diploid cells. By siRNA knock down experiments we could also demonstrate that NRP can support rDNA transcription in the absence of nucleolin. CONCLUSION: We have identified a new nucleolin variant over expressed in germ cells in rat and analyzed its domain structure. We attribute that the transcriptional activity of rDNA genes in the late spermatogenesis is due to the presence of this variant NRP. The expression of this variant in the germ cells in the absence of nucleolin, could have additional functions in the mammalian spermatogenesis which needs to be investigated further. BioMed Central 2009-07-01 /pmc/articles/PMC2711064/ /pubmed/19570216 http://dx.doi.org/10.1186/1471-2199-10-64 Text en Copyright © 2009 Chathoth et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chathoth, Keerthi T Ganesan, Gayatri Rao, MRS Identification of a novel nucleolin related protein (NRP) gene expressed during rat spermatogenesis |
title | Identification of a novel nucleolin related protein (NRP) gene expressed during rat spermatogenesis |
title_full | Identification of a novel nucleolin related protein (NRP) gene expressed during rat spermatogenesis |
title_fullStr | Identification of a novel nucleolin related protein (NRP) gene expressed during rat spermatogenesis |
title_full_unstemmed | Identification of a novel nucleolin related protein (NRP) gene expressed during rat spermatogenesis |
title_short | Identification of a novel nucleolin related protein (NRP) gene expressed during rat spermatogenesis |
title_sort | identification of a novel nucleolin related protein (nrp) gene expressed during rat spermatogenesis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2711064/ https://www.ncbi.nlm.nih.gov/pubmed/19570216 http://dx.doi.org/10.1186/1471-2199-10-64 |
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