Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Most animals are oviparous. However, the genes regulating egg shell formation remain not very clear. In this study, we found that Forkhead box transcription factor L2 (FoxL2) directly activated follicle cell protein 3C () to regulate chorion formation. and had a similar expression pattern, both highly expressed in the follicular cells of female adults. Knockdown of or also resulted in the same phenotypes: obesity and female infertility. RNA interference (RNAi) results suggested that is a downstream gene of Furthermore, transient expression showed that FoxL2 could directly activate the promoter. These results suggest that is a direct target gene of FoxL2. Depletion of or prevented normal chorion formation. Our results first revealed the functions of Fcp3C and FoxL2 in regulation of oocyte maturation in an oviparous animal.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493777 | PMC |
http://dx.doi.org/10.1098/rsob.170061 | DOI Listing |
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