Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS)
<p<Abstract</p< <p<Background</p< <p<The <it<pir </it<genes comprise the largest multi-gene family in <it<Plasmodium</it<, with members found in <it<P. vivax, P. knowlesi </it<and the rodent malaria species. Despite comprising up to 5...
Ausführliche Beschreibung
Autor*in: |
Lawton Jennifer [verfasserIn] Brugat Thibaut [verfasserIn] Yan Yam [verfasserIn] Reid Adam [verfasserIn] Böhme Ulrike [verfasserIn] Otto Thomas [verfasserIn] Pain Arnab [verfasserIn] Jackson Andrew [verfasserIn] Berriman Matthew [verfasserIn] Cunningham Deirdre [verfasserIn] Preiser Peter [verfasserIn] Langhorne Jean [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2012 |
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Übergeordnetes Werk: |
In: BMC Genomics - BMC, 2003, 13(2012), 1, p 125 |
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Übergeordnetes Werk: |
volume:13 ; year:2012 ; number:1, p 125 |
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DOI / URN: |
10.1186/1471-2164-13-125 |
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Katalog-ID: |
DOAJ026450380 |
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520 | |a <p<Abstract</p< <p<Background</p< <p<The <it<pir </it<genes comprise the largest multi-gene family in <it<Plasmodium</it<, with members found in <it<P. vivax, P. knowlesi </it<and the rodent malaria species. Despite comprising up to 5% of the genome, little is known about the functions of the proteins encoded by <it<pir </it<genes. <it<P. chabaudi </it<causes chronic infection in mice, which may be due to antigenic variation. In this model, <it<pir </it<genes are called <it<cir</it<s and may be involved in this mechanism, allowing evasion of host immune responses. In order to fully understand the role(s) of CIR proteins during <it<P. chabaudi </it<infection, a detailed characterization of the <it<cir </it<gene family was required.</p< <p<Results</p< <p<The <it<cir </it<repertoire was annotated and a detailed bioinformatic characterization of the encoded CIR proteins was performed. Two major sub-families were identified, which have been named A and B. Members of each sub-family displayed different amino acid motifs, and were thus predicted to have undergone functional divergence. In addition, the expression of the entire <it<cir </it<repertoire was analyzed via RNA sequencing and microarray. Up to 40% of the <it<cir </it<gene repertoire was expressed in the parasite population during infection, and dominant <it<cir </it<transcripts could be identified. In addition, some differences were observed in the pattern of expression between the <it<cir </it<subgroups at the peak of <it<P. chabaudi </it<infection. Finally, specific <it<cir </it<genes were expressed at different time points during asexual blood stages.</p< <p<Conclusions</p< <p<In conclusion, the large number of <it<cir </it<genes and their expression throughout the intraerythrocytic cycle of development indicates that CIR proteins are likely to be important for parasite survival. In particular, the detection of dominant <it<cir </it<transcripts at the peak of <it<P. chabaudi </it<infection supports the idea that CIR proteins are expressed, and could perform important functions in the biology of this parasite. Further application of the methodologies described here may allow the elucidation of CIR sub-family A and B protein functions, including their contribution to antigenic variation and immune evasion.</p< | ||
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10.1186/1471-2164-13-125 doi (DE-627)DOAJ026450380 (DE-599)DOAJ03f041523e364779a3eaf324e10d4807 DE-627 ger DE-627 rakwb eng TP248.13-248.65 QH426-470 Lawton Jennifer verfasserin aut Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<The <it<pir </it<genes comprise the largest multi-gene family in <it<Plasmodium</it<, with members found in <it<P. vivax, P. knowlesi </it<and the rodent malaria species. Despite comprising up to 5% of the genome, little is known about the functions of the proteins encoded by <it<pir </it<genes. <it<P. chabaudi </it<causes chronic infection in mice, which may be due to antigenic variation. In this model, <it<pir </it<genes are called <it<cir</it<s and may be involved in this mechanism, allowing evasion of host immune responses. In order to fully understand the role(s) of CIR proteins during <it<P. chabaudi </it<infection, a detailed characterization of the <it<cir </it<gene family was required.</p< <p<Results</p< <p<The <it<cir </it<repertoire was annotated and a detailed bioinformatic characterization of the encoded CIR proteins was performed. Two major sub-families were identified, which have been named A and B. Members of each sub-family displayed different amino acid motifs, and were thus predicted to have undergone functional divergence. In addition, the expression of the entire <it<cir </it<repertoire was analyzed via RNA sequencing and microarray. Up to 40% of the <it<cir </it<gene repertoire was expressed in the parasite population during infection, and dominant <it<cir </it<transcripts could be identified. In addition, some differences were observed in the pattern of expression between the <it<cir </it<subgroups at the peak of <it<P. chabaudi </it<infection. Finally, specific <it<cir </it<genes were expressed at different time points during asexual blood stages.</p< <p<Conclusions</p< <p<In conclusion, the large number of <it<cir </it<genes and their expression throughout the intraerythrocytic cycle of development indicates that CIR proteins are likely to be important for parasite survival. In particular, the detection of dominant <it<cir </it<transcripts at the peak of <it<P. chabaudi </it<infection supports the idea that CIR proteins are expressed, and could perform important functions in the biology of this parasite. Further application of the methodologies described here may allow the elucidation of CIR sub-family A and B protein functions, including their contribution to antigenic variation and immune evasion.</p< Biotechnology Genetics Brugat Thibaut verfasserin aut Yan Yam verfasserin aut Reid Adam verfasserin aut Böhme Ulrike verfasserin aut Otto Thomas verfasserin aut Pain Arnab verfasserin aut Jackson Andrew verfasserin aut Berriman Matthew verfasserin aut Cunningham Deirdre verfasserin aut Preiser Peter verfasserin aut Langhorne Jean verfasserin aut In BMC Genomics BMC, 2003 13(2012), 1, p 125 (DE-627)326644954 (DE-600)2041499-7 14712164 nnns volume:13 year:2012 number:1, p 125 https://doi.org/10.1186/1471-2164-13-125 kostenfrei https://doaj.org/article/03f041523e364779a3eaf324e10d4807 kostenfrei http://www.biomedcentral.com/1471-2164/13/125 kostenfrei https://doaj.org/toc/1471-2164 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2012 1, p 125 |
spelling |
10.1186/1471-2164-13-125 doi (DE-627)DOAJ026450380 (DE-599)DOAJ03f041523e364779a3eaf324e10d4807 DE-627 ger DE-627 rakwb eng TP248.13-248.65 QH426-470 Lawton Jennifer verfasserin aut Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<The <it<pir </it<genes comprise the largest multi-gene family in <it<Plasmodium</it<, with members found in <it<P. vivax, P. knowlesi </it<and the rodent malaria species. Despite comprising up to 5% of the genome, little is known about the functions of the proteins encoded by <it<pir </it<genes. <it<P. chabaudi </it<causes chronic infection in mice, which may be due to antigenic variation. In this model, <it<pir </it<genes are called <it<cir</it<s and may be involved in this mechanism, allowing evasion of host immune responses. In order to fully understand the role(s) of CIR proteins during <it<P. chabaudi </it<infection, a detailed characterization of the <it<cir </it<gene family was required.</p< <p<Results</p< <p<The <it<cir </it<repertoire was annotated and a detailed bioinformatic characterization of the encoded CIR proteins was performed. Two major sub-families were identified, which have been named A and B. Members of each sub-family displayed different amino acid motifs, and were thus predicted to have undergone functional divergence. In addition, the expression of the entire <it<cir </it<repertoire was analyzed via RNA sequencing and microarray. Up to 40% of the <it<cir </it<gene repertoire was expressed in the parasite population during infection, and dominant <it<cir </it<transcripts could be identified. In addition, some differences were observed in the pattern of expression between the <it<cir </it<subgroups at the peak of <it<P. chabaudi </it<infection. Finally, specific <it<cir </it<genes were expressed at different time points during asexual blood stages.</p< <p<Conclusions</p< <p<In conclusion, the large number of <it<cir </it<genes and their expression throughout the intraerythrocytic cycle of development indicates that CIR proteins are likely to be important for parasite survival. In particular, the detection of dominant <it<cir </it<transcripts at the peak of <it<P. chabaudi </it<infection supports the idea that CIR proteins are expressed, and could perform important functions in the biology of this parasite. Further application of the methodologies described here may allow the elucidation of CIR sub-family A and B protein functions, including their contribution to antigenic variation and immune evasion.</p< Biotechnology Genetics Brugat Thibaut verfasserin aut Yan Yam verfasserin aut Reid Adam verfasserin aut Böhme Ulrike verfasserin aut Otto Thomas verfasserin aut Pain Arnab verfasserin aut Jackson Andrew verfasserin aut Berriman Matthew verfasserin aut Cunningham Deirdre verfasserin aut Preiser Peter verfasserin aut Langhorne Jean verfasserin aut In BMC Genomics BMC, 2003 13(2012), 1, p 125 (DE-627)326644954 (DE-600)2041499-7 14712164 nnns volume:13 year:2012 number:1, p 125 https://doi.org/10.1186/1471-2164-13-125 kostenfrei https://doaj.org/article/03f041523e364779a3eaf324e10d4807 kostenfrei http://www.biomedcentral.com/1471-2164/13/125 kostenfrei https://doaj.org/toc/1471-2164 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2012 1, p 125 |
allfields_unstemmed |
10.1186/1471-2164-13-125 doi (DE-627)DOAJ026450380 (DE-599)DOAJ03f041523e364779a3eaf324e10d4807 DE-627 ger DE-627 rakwb eng TP248.13-248.65 QH426-470 Lawton Jennifer verfasserin aut Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<The <it<pir </it<genes comprise the largest multi-gene family in <it<Plasmodium</it<, with members found in <it<P. vivax, P. knowlesi </it<and the rodent malaria species. Despite comprising up to 5% of the genome, little is known about the functions of the proteins encoded by <it<pir </it<genes. <it<P. chabaudi </it<causes chronic infection in mice, which may be due to antigenic variation. In this model, <it<pir </it<genes are called <it<cir</it<s and may be involved in this mechanism, allowing evasion of host immune responses. In order to fully understand the role(s) of CIR proteins during <it<P. chabaudi </it<infection, a detailed characterization of the <it<cir </it<gene family was required.</p< <p<Results</p< <p<The <it<cir </it<repertoire was annotated and a detailed bioinformatic characterization of the encoded CIR proteins was performed. Two major sub-families were identified, which have been named A and B. Members of each sub-family displayed different amino acid motifs, and were thus predicted to have undergone functional divergence. In addition, the expression of the entire <it<cir </it<repertoire was analyzed via RNA sequencing and microarray. Up to 40% of the <it<cir </it<gene repertoire was expressed in the parasite population during infection, and dominant <it<cir </it<transcripts could be identified. In addition, some differences were observed in the pattern of expression between the <it<cir </it<subgroups at the peak of <it<P. chabaudi </it<infection. Finally, specific <it<cir </it<genes were expressed at different time points during asexual blood stages.</p< <p<Conclusions</p< <p<In conclusion, the large number of <it<cir </it<genes and their expression throughout the intraerythrocytic cycle of development indicates that CIR proteins are likely to be important for parasite survival. In particular, the detection of dominant <it<cir </it<transcripts at the peak of <it<P. chabaudi </it<infection supports the idea that CIR proteins are expressed, and could perform important functions in the biology of this parasite. Further application of the methodologies described here may allow the elucidation of CIR sub-family A and B protein functions, including their contribution to antigenic variation and immune evasion.</p< Biotechnology Genetics Brugat Thibaut verfasserin aut Yan Yam verfasserin aut Reid Adam verfasserin aut Böhme Ulrike verfasserin aut Otto Thomas verfasserin aut Pain Arnab verfasserin aut Jackson Andrew verfasserin aut Berriman Matthew verfasserin aut Cunningham Deirdre verfasserin aut Preiser Peter verfasserin aut Langhorne Jean verfasserin aut In BMC Genomics BMC, 2003 13(2012), 1, p 125 (DE-627)326644954 (DE-600)2041499-7 14712164 nnns volume:13 year:2012 number:1, p 125 https://doi.org/10.1186/1471-2164-13-125 kostenfrei https://doaj.org/article/03f041523e364779a3eaf324e10d4807 kostenfrei http://www.biomedcentral.com/1471-2164/13/125 kostenfrei https://doaj.org/toc/1471-2164 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2012 1, p 125 |
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10.1186/1471-2164-13-125 doi (DE-627)DOAJ026450380 (DE-599)DOAJ03f041523e364779a3eaf324e10d4807 DE-627 ger DE-627 rakwb eng TP248.13-248.65 QH426-470 Lawton Jennifer verfasserin aut Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<The <it<pir </it<genes comprise the largest multi-gene family in <it<Plasmodium</it<, with members found in <it<P. vivax, P. knowlesi </it<and the rodent malaria species. Despite comprising up to 5% of the genome, little is known about the functions of the proteins encoded by <it<pir </it<genes. <it<P. chabaudi </it<causes chronic infection in mice, which may be due to antigenic variation. In this model, <it<pir </it<genes are called <it<cir</it<s and may be involved in this mechanism, allowing evasion of host immune responses. In order to fully understand the role(s) of CIR proteins during <it<P. chabaudi </it<infection, a detailed characterization of the <it<cir </it<gene family was required.</p< <p<Results</p< <p<The <it<cir </it<repertoire was annotated and a detailed bioinformatic characterization of the encoded CIR proteins was performed. Two major sub-families were identified, which have been named A and B. Members of each sub-family displayed different amino acid motifs, and were thus predicted to have undergone functional divergence. In addition, the expression of the entire <it<cir </it<repertoire was analyzed via RNA sequencing and microarray. Up to 40% of the <it<cir </it<gene repertoire was expressed in the parasite population during infection, and dominant <it<cir </it<transcripts could be identified. In addition, some differences were observed in the pattern of expression between the <it<cir </it<subgroups at the peak of <it<P. chabaudi </it<infection. Finally, specific <it<cir </it<genes were expressed at different time points during asexual blood stages.</p< <p<Conclusions</p< <p<In conclusion, the large number of <it<cir </it<genes and their expression throughout the intraerythrocytic cycle of development indicates that CIR proteins are likely to be important for parasite survival. In particular, the detection of dominant <it<cir </it<transcripts at the peak of <it<P. chabaudi </it<infection supports the idea that CIR proteins are expressed, and could perform important functions in the biology of this parasite. Further application of the methodologies described here may allow the elucidation of CIR sub-family A and B protein functions, including their contribution to antigenic variation and immune evasion.</p< Biotechnology Genetics Brugat Thibaut verfasserin aut Yan Yam verfasserin aut Reid Adam verfasserin aut Böhme Ulrike verfasserin aut Otto Thomas verfasserin aut Pain Arnab verfasserin aut Jackson Andrew verfasserin aut Berriman Matthew verfasserin aut Cunningham Deirdre verfasserin aut Preiser Peter verfasserin aut Langhorne Jean verfasserin aut In BMC Genomics BMC, 2003 13(2012), 1, p 125 (DE-627)326644954 (DE-600)2041499-7 14712164 nnns volume:13 year:2012 number:1, p 125 https://doi.org/10.1186/1471-2164-13-125 kostenfrei https://doaj.org/article/03f041523e364779a3eaf324e10d4807 kostenfrei http://www.biomedcentral.com/1471-2164/13/125 kostenfrei https://doaj.org/toc/1471-2164 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2012 1, p 125 |
allfieldsSound |
10.1186/1471-2164-13-125 doi (DE-627)DOAJ026450380 (DE-599)DOAJ03f041523e364779a3eaf324e10d4807 DE-627 ger DE-627 rakwb eng TP248.13-248.65 QH426-470 Lawton Jennifer verfasserin aut Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<The <it<pir </it<genes comprise the largest multi-gene family in <it<Plasmodium</it<, with members found in <it<P. vivax, P. knowlesi </it<and the rodent malaria species. Despite comprising up to 5% of the genome, little is known about the functions of the proteins encoded by <it<pir </it<genes. <it<P. chabaudi </it<causes chronic infection in mice, which may be due to antigenic variation. In this model, <it<pir </it<genes are called <it<cir</it<s and may be involved in this mechanism, allowing evasion of host immune responses. In order to fully understand the role(s) of CIR proteins during <it<P. chabaudi </it<infection, a detailed characterization of the <it<cir </it<gene family was required.</p< <p<Results</p< <p<The <it<cir </it<repertoire was annotated and a detailed bioinformatic characterization of the encoded CIR proteins was performed. Two major sub-families were identified, which have been named A and B. Members of each sub-family displayed different amino acid motifs, and were thus predicted to have undergone functional divergence. In addition, the expression of the entire <it<cir </it<repertoire was analyzed via RNA sequencing and microarray. Up to 40% of the <it<cir </it<gene repertoire was expressed in the parasite population during infection, and dominant <it<cir </it<transcripts could be identified. In addition, some differences were observed in the pattern of expression between the <it<cir </it<subgroups at the peak of <it<P. chabaudi </it<infection. Finally, specific <it<cir </it<genes were expressed at different time points during asexual blood stages.</p< <p<Conclusions</p< <p<In conclusion, the large number of <it<cir </it<genes and their expression throughout the intraerythrocytic cycle of development indicates that CIR proteins are likely to be important for parasite survival. In particular, the detection of dominant <it<cir </it<transcripts at the peak of <it<P. chabaudi </it<infection supports the idea that CIR proteins are expressed, and could perform important functions in the biology of this parasite. Further application of the methodologies described here may allow the elucidation of CIR sub-family A and B protein functions, including their contribution to antigenic variation and immune evasion.</p< Biotechnology Genetics Brugat Thibaut verfasserin aut Yan Yam verfasserin aut Reid Adam verfasserin aut Böhme Ulrike verfasserin aut Otto Thomas verfasserin aut Pain Arnab verfasserin aut Jackson Andrew verfasserin aut Berriman Matthew verfasserin aut Cunningham Deirdre verfasserin aut Preiser Peter verfasserin aut Langhorne Jean verfasserin aut In BMC Genomics BMC, 2003 13(2012), 1, p 125 (DE-627)326644954 (DE-600)2041499-7 14712164 nnns volume:13 year:2012 number:1, p 125 https://doi.org/10.1186/1471-2164-13-125 kostenfrei https://doaj.org/article/03f041523e364779a3eaf324e10d4807 kostenfrei http://www.biomedcentral.com/1471-2164/13/125 kostenfrei https://doaj.org/toc/1471-2164 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2012 1, p 125 |
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Lawton Jennifer @@aut@@ Brugat Thibaut @@aut@@ Yan Yam @@aut@@ Reid Adam @@aut@@ Böhme Ulrike @@aut@@ Otto Thomas @@aut@@ Pain Arnab @@aut@@ Jackson Andrew @@aut@@ Berriman Matthew @@aut@@ Cunningham Deirdre @@aut@@ Preiser Peter @@aut@@ Langhorne Jean @@aut@@ |
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Lawton Jennifer misc TP248.13-248.65 misc QH426-470 misc Biotechnology misc Genetics Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) |
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TP248.13-248.65 QH426-470 Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) |
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Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) |
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Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) |
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Lawton Jennifer |
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Lawton Jennifer Brugat Thibaut Yan Yam Reid Adam Böhme Ulrike Otto Thomas Pain Arnab Jackson Andrew Berriman Matthew Cunningham Deirdre Preiser Peter Langhorne Jean |
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characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(as) |
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TP248.13-248.65 |
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Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) |
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<p<Abstract</p< <p<Background</p< <p<The <it<pir </it<genes comprise the largest multi-gene family in <it<Plasmodium</it<, with members found in <it<P. vivax, P. knowlesi </it<and the rodent malaria species. Despite comprising up to 5% of the genome, little is known about the functions of the proteins encoded by <it<pir </it<genes. <it<P. chabaudi </it<causes chronic infection in mice, which may be due to antigenic variation. In this model, <it<pir </it<genes are called <it<cir</it<s and may be involved in this mechanism, allowing evasion of host immune responses. In order to fully understand the role(s) of CIR proteins during <it<P. chabaudi </it<infection, a detailed characterization of the <it<cir </it<gene family was required.</p< <p<Results</p< <p<The <it<cir </it<repertoire was annotated and a detailed bioinformatic characterization of the encoded CIR proteins was performed. Two major sub-families were identified, which have been named A and B. Members of each sub-family displayed different amino acid motifs, and were thus predicted to have undergone functional divergence. In addition, the expression of the entire <it<cir </it<repertoire was analyzed via RNA sequencing and microarray. Up to 40% of the <it<cir </it<gene repertoire was expressed in the parasite population during infection, and dominant <it<cir </it<transcripts could be identified. In addition, some differences were observed in the pattern of expression between the <it<cir </it<subgroups at the peak of <it<P. chabaudi </it<infection. Finally, specific <it<cir </it<genes were expressed at different time points during asexual blood stages.</p< <p<Conclusions</p< <p<In conclusion, the large number of <it<cir </it<genes and their expression throughout the intraerythrocytic cycle of development indicates that CIR proteins are likely to be important for parasite survival. In particular, the detection of dominant <it<cir </it<transcripts at the peak of <it<P. chabaudi </it<infection supports the idea that CIR proteins are expressed, and could perform important functions in the biology of this parasite. Further application of the methodologies described here may allow the elucidation of CIR sub-family A and B protein functions, including their contribution to antigenic variation and immune evasion.</p< |
abstractGer |
<p<Abstract</p< <p<Background</p< <p<The <it<pir </it<genes comprise the largest multi-gene family in <it<Plasmodium</it<, with members found in <it<P. vivax, P. knowlesi </it<and the rodent malaria species. Despite comprising up to 5% of the genome, little is known about the functions of the proteins encoded by <it<pir </it<genes. <it<P. chabaudi </it<causes chronic infection in mice, which may be due to antigenic variation. In this model, <it<pir </it<genes are called <it<cir</it<s and may be involved in this mechanism, allowing evasion of host immune responses. In order to fully understand the role(s) of CIR proteins during <it<P. chabaudi </it<infection, a detailed characterization of the <it<cir </it<gene family was required.</p< <p<Results</p< <p<The <it<cir </it<repertoire was annotated and a detailed bioinformatic characterization of the encoded CIR proteins was performed. Two major sub-families were identified, which have been named A and B. Members of each sub-family displayed different amino acid motifs, and were thus predicted to have undergone functional divergence. In addition, the expression of the entire <it<cir </it<repertoire was analyzed via RNA sequencing and microarray. Up to 40% of the <it<cir </it<gene repertoire was expressed in the parasite population during infection, and dominant <it<cir </it<transcripts could be identified. In addition, some differences were observed in the pattern of expression between the <it<cir </it<subgroups at the peak of <it<P. chabaudi </it<infection. Finally, specific <it<cir </it<genes were expressed at different time points during asexual blood stages.</p< <p<Conclusions</p< <p<In conclusion, the large number of <it<cir </it<genes and their expression throughout the intraerythrocytic cycle of development indicates that CIR proteins are likely to be important for parasite survival. In particular, the detection of dominant <it<cir </it<transcripts at the peak of <it<P. chabaudi </it<infection supports the idea that CIR proteins are expressed, and could perform important functions in the biology of this parasite. Further application of the methodologies described here may allow the elucidation of CIR sub-family A and B protein functions, including their contribution to antigenic variation and immune evasion.</p< |
abstract_unstemmed |
<p<Abstract</p< <p<Background</p< <p<The <it<pir </it<genes comprise the largest multi-gene family in <it<Plasmodium</it<, with members found in <it<P. vivax, P. knowlesi </it<and the rodent malaria species. Despite comprising up to 5% of the genome, little is known about the functions of the proteins encoded by <it<pir </it<genes. <it<P. chabaudi </it<causes chronic infection in mice, which may be due to antigenic variation. In this model, <it<pir </it<genes are called <it<cir</it<s and may be involved in this mechanism, allowing evasion of host immune responses. In order to fully understand the role(s) of CIR proteins during <it<P. chabaudi </it<infection, a detailed characterization of the <it<cir </it<gene family was required.</p< <p<Results</p< <p<The <it<cir </it<repertoire was annotated and a detailed bioinformatic characterization of the encoded CIR proteins was performed. Two major sub-families were identified, which have been named A and B. Members of each sub-family displayed different amino acid motifs, and were thus predicted to have undergone functional divergence. In addition, the expression of the entire <it<cir </it<repertoire was analyzed via RNA sequencing and microarray. Up to 40% of the <it<cir </it<gene repertoire was expressed in the parasite population during infection, and dominant <it<cir </it<transcripts could be identified. In addition, some differences were observed in the pattern of expression between the <it<cir </it<subgroups at the peak of <it<P. chabaudi </it<infection. Finally, specific <it<cir </it<genes were expressed at different time points during asexual blood stages.</p< <p<Conclusions</p< <p<In conclusion, the large number of <it<cir </it<genes and their expression throughout the intraerythrocytic cycle of development indicates that CIR proteins are likely to be important for parasite survival. In particular, the detection of dominant <it<cir </it<transcripts at the peak of <it<P. chabaudi </it<infection supports the idea that CIR proteins are expressed, and could perform important functions in the biology of this parasite. Further application of the methodologies described here may allow the elucidation of CIR sub-family A and B protein functions, including their contribution to antigenic variation and immune evasion.</p< |
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Characterization and gene expression analysis of the <it<cir </it<multi-gene family of <it<plasmodium chabaudi chabaudi </it<(AS) |
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https://doi.org/10.1186/1471-2164-13-125 https://doaj.org/article/03f041523e364779a3eaf324e10d4807 http://www.biomedcentral.com/1471-2164/13/125 https://doaj.org/toc/1471-2164 |
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In addition, the expression of the entire <it<cir </it<repertoire was analyzed via RNA sequencing and microarray. Up to 40% of the <it<cir </it<gene repertoire was expressed in the parasite population during infection, and dominant <it<cir </it<transcripts could be identified. In addition, some differences were observed in the pattern of expression between the <it<cir </it<subgroups at the peak of <it<P. chabaudi </it<infection. Finally, specific <it<cir </it<genes were expressed at different time points during asexual blood stages.</p< <p<Conclusions</p< <p<In conclusion, the large number of <it<cir </it<genes and their expression throughout the intraerythrocytic cycle of development indicates that CIR proteins are likely to be important for parasite survival. In particular, the detection of dominant <it<cir </it<transcripts at the peak of <it<P. chabaudi </it<infection supports the idea that CIR proteins are expressed, and could perform important functions in the biology of this parasite. 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