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. 2015 May 5;10(5):e0124117. doi: 10.1371/journal.pone.0124117

Table 2. Short-listed candidate genes located in the PNR1 QTL on Chr 12.

Index Symbol Gene Microarray Microarray Literature Significance #
BM vs. PE Blood vs. PE
FC* FC*
1 Hif1a Hypoxia inducible factor 1, alpha subunit 4.72 7.43 [29]
2 Prkch Protein kinase C, eta 2.20 2.37 [23]
3 Fntb Farnesyltransferase, CAAX box, beta -1.91 -3.63 [22]
4 Dhrs7 Dehydrogenase/reductase SDR family member 7 -2.79 [34]
5 1200003C05Rik RIKEN cDNA 1200003C05 gene -1.65 -1.71
6 Ppm1a Protein phosphatase 1A -1.886 [35]
7 Snapc1 snRNA-activating protein complex subunit 1 1.493 1.58
8 Max Max protein 1.79 [36]
9 Mnat1 Menage a trois 1/ cyclin H assembly factor -1.55
10 Daam1 Disheveled-associated activator of morphogenesis [37]
11 Rhoj Ras homolog family member J [38]
12 Sgpp1 Sphingosine-1-phosphate phosphatase 1 [39]
13 Syne2 Spectrin repeat containing, nuclear envelope 2; Nesp2g [40]
14 Esr2 Estrogen receptor 2 (beta) [41]
15 Akap5 A kinase (PRKA) anchor protein 5 [42]
16 Gpx2 Glutathione peroxidase 2 [43]

Sixteen genes were prioritized through a selective literature search, inclusion in 2 NR gene expression studies, and presence of SNPs differing in the parental strains.

(-) indicates mRNAs were downregulated as PMNs transit from BM to PE and Blood to PE. BM—Bone Marrow; PE—Peritoneum; FC—Fold Change.

* FC significant at p<0.05.

#Using PubMed, each candidate gene was searched using the “AND” function with 11 terms selected to be relevant to NR including “neutrophil”, “neutrophil recruitment”, “neutrophil activation”, “neutrophil infiltration”, “neutrophil chemotaxis”, “innate immunity”, “cell migration”, “actin”, “cytoskeleton”, and “GTPases”. Bolded genes show significance with both microarray data sets.