Title:Investigating Key Genes in Type 2 Diabetes Mellitus via Combining mAP-KL and Mutual Information Network
VOLUME: 12 ISSUE: 5
Author(s):Guiyan Chen, Weihai Qiu, Shuze Xia and Lijuan Wang*
Affiliation:Department of Endocrinology, Binzhou People’s Hospital, Binzhou 256600, Shandong Province, Department of Endocrinology, Binzhou People’s Hospital, Binzhou 256600, Shandong Province, Department of Endocrinology, Binzhou People’s Hospital, Binzhou 256600, Shandong Province, Department of Endocrinology, The Second Hospital of Jilin University, No. 218 Ziqiang Street, Nanguan district, Changchun 130000, Jilin Province
Keywords:Type 2 diabetes mellitus, mAP-KL, cluster, mutual information network, support vector machines, hub genes.
Abstract:Background: The molecular mechanism of the type 2 diabetes mellitus (T2DM) remains
unclear.
Objective: This research aimed to investigate key genes in T2DM via combining mAP-KL and mutual
information network (MIN) and give great insights to reveal pathological mechanism underlying this
disease.
Methods: First of all, the data of gene expression profile of T2DM were recruited and preprocessed;
then mAP-KL was implemented to investigate clusters and exemplars in T2DM; in the following,
support vector machines (SVM) model was selected to evaluate the classification performance of mAPKL;
finally, MIN construction and topological analysis were performed to investigate key genes.
Results: A total of 20,541 gene symbols were obtained from expression profile of T2DM. By applying
mAP-KL, 12 clusters were identified. From Cluster 1 to Cluster 12, their exemplars were OGT, TTC22,
LIMCH1, NENF, ROMO1, RGL2, TCF7L1, KRTAP4-4, POLR2F, KIF22, NDUFB11, and AGL,
respectively. The results of evaluation by SVM model indicated that the mAP-KL methodology was
feasible and suitable for identifying exemplars of T2DM. Finally, MIN construction and topological
analysis indicated that there were four hub genes (degree centrality ≥ 100): TCF7L1 (degree = 104),
LIMCH1 (degree = 102), NENF (degree = 101), TTC22 (degree = 101), which might be potentially
novel predictive and prognostic markers for T2DM.
Conclusion: We predict these hub genes (such as TCF7L1 and LIMCH1) might play key roles during
the occurrence and development of T2DM and are potentially novel predictive and prognostic markers
for T2DM.
