Forward and reverse primers, and 2 mL of template cDNA. PCR amplification was performed under the following conditions: 95uC for 30 s, followed by 40 cycles of 95uC for 5 s and 60uC for 30 s, at last by 55uC for 30 s. The expression of four interesting genes were normalized against an internal reference gene, b-actin. Primers were designed using Beacon Designer 7.7 software (primer sequences upon Docosahexaenoyl ethanolamide request) (Table S4). For caste-specific expression assay, expression in workers was used as the calibrator for each gene. The relative gene expression was calculated using the 22DDCt method 25033180 [50]. All qPCR were repeated in three biological and three technical replications. Differences in expression level of the four genes among workers, soldiers and larvae were tested for significance by a one-way ANOVA with means separated using Tukey’s HSD (SPSS Inc., 1989?002).Figure S2 Length distribution of CDS predicted from ESTScan. The x-axis shows read size and the y-axis shows the number of reads for each given size. (TIF)Top BLAST hits from NCBI nr database. BLAST results against the NCBI nr database for all the distinct sequences with a cut-off E-value above 1025 are shown. (XLSX)Table S1 Table S2 BLAST hits from the four databases (nr,KEGG, COG, Swiss-Prot). (XLSX)Table S3 Predicted EST-SSRs in the head transcriptome of Odontotermes formosanus. (XLSX) Table S4 Interesting gene ID in the head transcriptome and primers used for qPCR. (DOC)Data DepositionThe Illumina sequencing reads of worker heads of O. formosanus were submitted to NCBI Sequence Read Archive under the accession number of SRA055431.AcknowledgmentsWe thank the technical support for Illumina sequencing and initial data analysis from Beijing Genome Institute at Shenzhen, China. We thank Drs. Keyan Zhu-Salzman and Weiwei Zheng, and the anonymous reviewers for providing valuable comments on earlier drafts of this manuscript.Supporting InformationFigure S1 Length distribution of CDS predicted from BLAST. The x-axis shows read size and the y-axis shows the number of reads for each given size. (TIF)Author ContributionsConceived and designed the experiments: QH PS XZ CL. Performed the experiments: QH PS. Analyzed the data: QH PS XZ CL. Contributed reagents/materials/analysis tools: QH PS CL. Wrote the 
paper: QH PS XZ CL.
Microtubules play an indispensable role in subcellular processes such as cell movement, cell division and intracellular transportation. In turn, these processes are known to play a role in other biological phenomena such as wound healing, and cancer metastasis. Extracting information about the organization of microtubules in different cell lines could potentially shed light on the roles of microtubule associated proteins in that organization. While limited information is available about variation in microtubule distributions [1,2], information on those distributions in intact cells for different cell lines has not been readily available. Most microtubule studies have focused on dynamics and interactions with drugs and microtubule associated proteins [3?6]. We believe that the ability to obtain Licochalcone-A reliable estimates of the overall organization of microtubules in whole cells could allow quantification of their dependency on different pertubagens, drugs, mechanical stimuli, etc.Electron microscopy can be used to trace microtubules, but the specimen preparation for imaging does not allow for intact cells to be imaged. Fluorescence microscopy can be used to image intact cells, but mic.Forward and reverse primers, and 2 mL of template cDNA. PCR amplification was performed under the following conditions: 95uC for 30 s, followed by 40 cycles of 95uC for 5 s and 60uC for 30 s, at last by 55uC for 30 s. The expression of four interesting genes were normalized against an internal reference gene, b-actin. Primers were designed using Beacon Designer 7.7 software (primer sequences upon request) (Table S4). For caste-specific expression assay, expression in workers was used as the calibrator for each gene. The relative gene expression was calculated using the 22DDCt method 25033180 [50]. All qPCR were repeated in three biological and three technical replications. Differences in expression level of the four genes among workers, soldiers and larvae were tested for significance by a one-way ANOVA with means separated using Tukey’s HSD (SPSS Inc., 1989?002).Figure S2 Length distribution of CDS predicted from ESTScan. The x-axis shows read size and the y-axis shows the number of reads for 
each given size. (TIF)Top BLAST hits from NCBI nr database. BLAST results against the NCBI nr database for all the distinct sequences with a cut-off E-value above 1025 are shown. (XLSX)Table S1 Table S2 BLAST hits from the four databases (nr,KEGG, COG, Swiss-Prot). (XLSX)Table S3 Predicted EST-SSRs in the head transcriptome of Odontotermes formosanus. (XLSX) Table S4 Interesting gene ID in the head transcriptome and primers used for qPCR. (DOC)Data DepositionThe Illumina sequencing reads of worker heads of O. formosanus were submitted to NCBI Sequence Read Archive under the accession number of SRA055431.AcknowledgmentsWe thank the technical support for Illumina sequencing and initial data analysis from Beijing Genome Institute at Shenzhen, China. We thank Drs. Keyan Zhu-Salzman and Weiwei Zheng, and the anonymous reviewers for providing valuable comments on earlier drafts of this manuscript.Supporting InformationFigure S1 Length distribution of CDS predicted from BLAST. The x-axis shows read size and the y-axis shows the number of reads for each given size. (TIF)Author ContributionsConceived and designed the experiments: QH PS XZ CL. Performed the experiments: QH PS. Analyzed the data: QH PS XZ CL. Contributed reagents/materials/analysis tools: QH PS CL. Wrote the paper: QH PS XZ CL.
Microtubules play an indispensable role in subcellular processes such as cell movement, cell division and intracellular transportation. In turn, these processes are known to play a role in other biological phenomena such as wound healing, and cancer metastasis. Extracting information about the organization of microtubules in different cell lines could potentially shed light on the roles of microtubule associated proteins in that organization. While limited information is available about variation in microtubule distributions [1,2], information on those distributions in intact cells for different cell lines has not been readily available. Most microtubule studies have focused on dynamics and interactions with drugs and microtubule associated proteins [3?6]. We believe that the ability to obtain reliable estimates of the overall organization of microtubules in whole cells could allow quantification of their dependency on different pertubagens, drugs, mechanical stimuli, etc.Electron microscopy can be used to trace microtubules, but the specimen preparation for imaging does not allow for intact cells to be imaged. Fluorescence microscopy can be used to image intact cells, but mic.