2017
DOI: 10.1016/j.theriogenology.2017.05.019
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Study of lysophosphatidic acid receptors (LPARs) in buffalo uterus demonstrated upregulation of LPAR1 and LPAR6 in early pregnancy

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Cited by 8 publications
(5 citation statements)
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“…We also detected the DGKG gene, which affects insulin signalling and lipid metabolism, and is a regulator of diacylglycerol and phosphatidic acid, which are important mediators of signal transduction (Sinha et al., 2020). We detected several candidate genes through the xp‐EHH analysis that were previously reported in other livestock, like PITX1 and KHDRBS1 in goats (Ma et al., 2017; Sayre, 2010); LPAR6 in buffaloes (Sadam et al., 2017); RTL1 in pigs (Yang et al., 2009); LRRC18 and CLDN17 in horses (Al Abri et al., 2018); and CLDN8, CLDN17 and MATN1 in cattle (Araujo et al., 2009; Campos et al., 2017; Kijas et al., 2006).…”
Section: Discussionmentioning
confidence: 75%
“…We also detected the DGKG gene, which affects insulin signalling and lipid metabolism, and is a regulator of diacylglycerol and phosphatidic acid, which are important mediators of signal transduction (Sinha et al., 2020). We detected several candidate genes through the xp‐EHH analysis that were previously reported in other livestock, like PITX1 and KHDRBS1 in goats (Ma et al., 2017; Sayre, 2010); LPAR6 in buffaloes (Sadam et al., 2017); RTL1 in pigs (Yang et al., 2009); LRRC18 and CLDN17 in horses (Al Abri et al., 2018); and CLDN8, CLDN17 and MATN1 in cattle (Araujo et al., 2009; Campos et al., 2017; Kijas et al., 2006).…”
Section: Discussionmentioning
confidence: 75%
“…Membrane proteins (detergent‐soluble hydrophobic membrane proteins) were extracted according to the manufacturer's instructions of the Membrane Protein Extraction Kit (Boster Bio, Pleasanton, CA, USA) as described previously (Sadam et al., ). Lipid raft proteins were isolated using a lipid raft isolation kit (Sigma‐Aldrich, St. Louis, MO, USA), following the manufacturer's instructions.…”
Section: Methodsmentioning
confidence: 99%
“…The amplification was carried out in 20 µl volume reaction mixture containing 10 µl (2×) master mix (Fast SYBR Green qRT‐PCR Master Mix), 1 µl (10 µM) gene‐specific forward and reverse primers, 2 µl cDNA template and 6µl nuclease‐free water and by following thermal profile of Fast SYBR Green Master Mix: 95°C for 20 s, followed by 40 cycles of 95°C for 3 s and 57–60°C for 30 s. Non‐template control was included in each run. The GAPDH gene, a housekeeping gene, was used as an endogenous control for the analysis of data as it is the most widely used (Davies et al, ; Lee et al, ; Sadam et al, ; Verma et al, ). Hence, relative expression of (i) GAPDH , as endogenous control, and (ii) LGALS1 , LGALS3BP , LGALS9 , SLC2A1 , SLC5A11 , MUC1, CTSL and CST3 genes as target genes was carried out, in both pregnancy stages as well as in the nonpregnant stage (calibrator group).…”
Section: Methodsmentioning
confidence: 99%