The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation
Tang, X.-Y., Zou, W.-B., Masson, E., Hu, L.-H., Ferec, C., Chen, J.-M., Li, Z.-S., Liao, Z.
BMJ Publishing Group
Published 2018
BMJ Publishing Group
Published 2018
| Publication Date: |
2018-06-08
|
|---|---|
| Publisher: |
BMJ Publishing Group
|
| Print ISSN: |
0017-5749
|
| Electronic ISSN: |
1468-3288
|
| Topics: |
Medicine
|
| Keywords: |
Gut
|
| Published by: |
| _version_ | 1836398964214071296 |
|---|---|
| autor | Tang, X.-Y., Zou, W.-B., Masson, E., Hu, L.-H., Ferec, C., Chen, J.-M., Li, Z.-S., Liao, Z. |
| beschreibung | We read with great interest the article by Rosendahl et al 1 reporting the identification of CTRB1-CTRB2 (chymotrypsin B1 and chymotrypsin B2) as a new chronic pancreatitis (CP) risk locus by means of genome-wide association study, with the lead single nucleotide polymorphism (SNP) rs8055167 having an OR of 1.35. Moreover, they found that a previously reported 16.6 kb inversion in the CTRB1-CTRB2 locus 2 was in linkage disequilibrium with the CP-associated SNPs and optimally tagged by rs8048956. Furthermore, they provided in silico and in vivo evidence showing that the inversion variant changes the expression ratio of the CTRB1 and CTRB2 isoforms, the major risk allele being associated with increased CTRB1 and decreased CTRB2 mRNA expression as compared with the minor allele. Finally, they provided in vitro evidence that CTRB1 was less efficient in degrading anionic trypsinogen (PRSS2) than CTRB2 (note that rapid degradation of PRSS2 conferred by a PRSS2 missense... |
| citation_standardnr | 6278859 |
| datenlieferant | ipn_articles |
| feed_id | 3103 |
| feed_publisher | BMJ Publishing Group |
| feed_publisher_url | http://www.bmj.com/ |
| insertion_date | 2018-06-08 |
| journaleissn | 1468-3288 |
| journalissn | 0017-5749 |
| publikationsjahr_anzeige | 2018 |
| publikationsjahr_facette | 2018 |
| publikationsjahr_intervall | 7984:2015-2019 |
| publikationsjahr_sort | 2018 |
| publisher | BMJ Publishing Group |
| quelle | Gut |
| relation | http://gut.bmj.com/cgi/content/short/67/7/1368?rss=1 |
| schlagwort | Gut |
| search_space | articles |
| shingle_author_1 | Tang, X.-Y., Zou, W.-B., Masson, E., Hu, L.-H., Ferec, C., Chen, J.-M., Li, Z.-S., Liao, Z. |
| shingle_author_2 | Tang, X.-Y., Zou, W.-B., Masson, E., Hu, L.-H., Ferec, C., Chen, J.-M., Li, Z.-S., Liao, Z. |
| shingle_author_3 | Tang, X.-Y., Zou, W.-B., Masson, E., Hu, L.-H., Ferec, C., Chen, J.-M., Li, Z.-S., Liao, Z. |
| shingle_author_4 | Tang, X.-Y., Zou, W.-B., Masson, E., Hu, L.-H., Ferec, C., Chen, J.-M., Li, Z.-S., Liao, Z. |
| shingle_catch_all_1 | The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation Gut We read with great interest the article by Rosendahl et al 1 reporting the identification of CTRB1-CTRB2 (chymotrypsin B1 and chymotrypsin B2) as a new chronic pancreatitis (CP) risk locus by means of genome-wide association study, with the lead single nucleotide polymorphism (SNP) rs8055167 having an OR of 1.35. Moreover, they found that a previously reported 16.6 kb inversion in the CTRB1-CTRB2 locus 2 was in linkage disequilibrium with the CP-associated SNPs and optimally tagged by rs8048956. Furthermore, they provided in silico and in vivo evidence showing that the inversion variant changes the expression ratio of the CTRB1 and CTRB2 isoforms, the major risk allele being associated with increased CTRB1 and decreased CTRB2 mRNA expression as compared with the minor allele. Finally, they provided in vitro evidence that CTRB1 was less efficient in degrading anionic trypsinogen (PRSS2) than CTRB2 (note that rapid degradation of PRSS2 conferred by a PRSS2 missense... Tang, X.-Y., Zou, W.-B., Masson, E., Hu, L.-H., Ferec, C., Chen, J.-M., Li, Z.-S., Liao, Z. BMJ Publishing Group 0017-5749 00175749 1468-3288 14683288 |
| shingle_catch_all_2 | The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation Gut We read with great interest the article by Rosendahl et al 1 reporting the identification of CTRB1-CTRB2 (chymotrypsin B1 and chymotrypsin B2) as a new chronic pancreatitis (CP) risk locus by means of genome-wide association study, with the lead single nucleotide polymorphism (SNP) rs8055167 having an OR of 1.35. Moreover, they found that a previously reported 16.6 kb inversion in the CTRB1-CTRB2 locus 2 was in linkage disequilibrium with the CP-associated SNPs and optimally tagged by rs8048956. Furthermore, they provided in silico and in vivo evidence showing that the inversion variant changes the expression ratio of the CTRB1 and CTRB2 isoforms, the major risk allele being associated with increased CTRB1 and decreased CTRB2 mRNA expression as compared with the minor allele. Finally, they provided in vitro evidence that CTRB1 was less efficient in degrading anionic trypsinogen (PRSS2) than CTRB2 (note that rapid degradation of PRSS2 conferred by a PRSS2 missense... Tang, X.-Y., Zou, W.-B., Masson, E., Hu, L.-H., Ferec, C., Chen, J.-M., Li, Z.-S., Liao, Z. BMJ Publishing Group 0017-5749 00175749 1468-3288 14683288 |
| shingle_catch_all_3 | The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation Gut We read with great interest the article by Rosendahl et al 1 reporting the identification of CTRB1-CTRB2 (chymotrypsin B1 and chymotrypsin B2) as a new chronic pancreatitis (CP) risk locus by means of genome-wide association study, with the lead single nucleotide polymorphism (SNP) rs8055167 having an OR of 1.35. Moreover, they found that a previously reported 16.6 kb inversion in the CTRB1-CTRB2 locus 2 was in linkage disequilibrium with the CP-associated SNPs and optimally tagged by rs8048956. Furthermore, they provided in silico and in vivo evidence showing that the inversion variant changes the expression ratio of the CTRB1 and CTRB2 isoforms, the major risk allele being associated with increased CTRB1 and decreased CTRB2 mRNA expression as compared with the minor allele. Finally, they provided in vitro evidence that CTRB1 was less efficient in degrading anionic trypsinogen (PRSS2) than CTRB2 (note that rapid degradation of PRSS2 conferred by a PRSS2 missense... Tang, X.-Y., Zou, W.-B., Masson, E., Hu, L.-H., Ferec, C., Chen, J.-M., Li, Z.-S., Liao, Z. BMJ Publishing Group 0017-5749 00175749 1468-3288 14683288 |
| shingle_catch_all_4 | The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation Gut We read with great interest the article by Rosendahl et al 1 reporting the identification of CTRB1-CTRB2 (chymotrypsin B1 and chymotrypsin B2) as a new chronic pancreatitis (CP) risk locus by means of genome-wide association study, with the lead single nucleotide polymorphism (SNP) rs8055167 having an OR of 1.35. Moreover, they found that a previously reported 16.6 kb inversion in the CTRB1-CTRB2 locus 2 was in linkage disequilibrium with the CP-associated SNPs and optimally tagged by rs8048956. Furthermore, they provided in silico and in vivo evidence showing that the inversion variant changes the expression ratio of the CTRB1 and CTRB2 isoforms, the major risk allele being associated with increased CTRB1 and decreased CTRB2 mRNA expression as compared with the minor allele. Finally, they provided in vitro evidence that CTRB1 was less efficient in degrading anionic trypsinogen (PRSS2) than CTRB2 (note that rapid degradation of PRSS2 conferred by a PRSS2 missense... Tang, X.-Y., Zou, W.-B., Masson, E., Hu, L.-H., Ferec, C., Chen, J.-M., Li, Z.-S., Liao, Z. BMJ Publishing Group 0017-5749 00175749 1468-3288 14683288 |
| shingle_title_1 | The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation |
| shingle_title_2 | The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation |
| shingle_title_3 | The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation |
| shingle_title_4 | The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation |
| timestamp | 2025-06-30T23:35:26.683Z |
| titel | The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation |
| titel_suche | The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation |
| topic | WW-YZ |
| uid | ipn_articles_6278859 |