Nutrient deficiency stresses often occur simultaneously in soil. Thus,it’s necessary to investigate the mechanisms underlying plant responses to multiple stresses through identification of some key stress-responsive genes. Quantitative real-time PCR(qRT-PCR)is essential for detecting the expression of the interested genes,of which the selection of suitable reference genes is a crucial step before qRT-PCR. To date,reliable reference genes to normalize qRT-PCR data under different nutrient deficiencies have not been reported in plants. In this study,expression of ten candidate reference genes was detected in leaves and roots of rapeseed(Brassica napus L.)after implementing different nutrient deficiencies for 14 days. These candidate genes,included two traditionally used reference genes and eight genes selected from an RNASeqdataset. Two software packages(Ge Norm,Norm Finder)were employed to evaluate candidate gene stability. Results showed that VHA-E1 was the highest-ranked gene in leaves of nutrient-deficient rapeseed,while VHA-G1 and UBC21 were most stable in nutrient-deficient roots. When rapeseed leaves and roots were combined,UBC21,HTB1,VHA-G1 and ACT7 were most stable among all samples. To evaluate the stabilities of the highest-ranked genes,the relative expression of two target genes,Bn Trx1;1 and Bn Pht1;3 were further determined. The results showed that the relative expression of Bn Trx1;1 depended on reference gene selection,suggesting that it’s necessary to evaluate the stability of reference gene prior to qRT-PCR. This study provides suitable reference genes for gene expression analysis of rapeseed responses to different nutrient deficiencies,which is essential for elucidation of mechanisms underlying rapeseed responses to multiple nutrient deficiency stresses. Thus, it’s necessary to investigate the mechanisms underlying plant responses to multiple stresses through identification of some key stress-responsive genes. Quantitative real-time PCR (qRT-PCR) is essential for detecting the expression of the interested genes, of which the selection of suitable reference genes is a crucial step before qRT-PCR. In this study, expression of ten candidate reference genes was detected in leaves and roots of rapeseed (Brassica napus L.) after implementing different nutrient deficiencies for 14 days. These candidate genes included two traditionally used reference genes and eight genes selected from an RNASeqdataset. Two software packages (Ge Norm, Norm Finder) were employed to evaluate candidate gene stability. Results showed that VHA-E1 was the highest-ranked gene in leave s of nutrient-deficient rapeseed, while while VHA-G1 and UBC21 were most stable among all-samples. When evaluate the performance of rapeseed leaves and roots, UBC21, HTB1, VHA-G1 and ACT7 were most stable among all samples. of the highest-ranked genes, the relative expression of two target genes, Bn Trx1; 1 and Bn Pht1; 3 were further determined. The results showed that the relative expression of Bn Trx1; 1 depended on reference gene selection, suggesting that it’s necessary to evaluate the stability of reference gene for gene expression analysis of rapeseed responses to different nutrient deficiencies, which is essential for elucidation of mechanisms underlying rapeseed responses to multiple nutrient deficiency stresses.