Selection of reference genes for expression analysis in the potato psyllid, Bactericera cockerelli

被引:34
|
作者
Ibanez, F. [1 ]
Tamborindeguy, C. [1 ]
机构
[1] Texas A&M Univ, Dept Entomol, College Stn, TX 77843 USA
基金
美国食品与农业研究所;
关键词
Psyllids; Bactericera cockerelli; Liberibacter; reference genes; gene expression; polymerase chain reaction; RHODNIUS-PROLIXUS HEMIPTERA; CANDIDATUS LIBERIBACTER SOLANACEARUM; HOUSEKEEPING GENES; RNA INTERFERENCE; SALIVARY-GLAND; APIS-MELLIFERA; ZEBRA CHIP; RT-PCR; VALIDATION; DISEASE;
D O I
10.1111/imb.12219
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The selection of reference genes is a crucial step for quantitative real-time PCR analyses and increasingly the use of more than one reference gene for accurate and reliable normalization is being recommended. In this study, a set of six genes was selected and their stability was assessed in different life stages and female organs of Bactericera cockerelli harbouring or not the bacterial pathogen 'Candidatus Liberibacter solanacearum' (Lso) haplotype B. The stability of each gene was determined using the BESTKEEPER, NORMFINDER and GENORM programs. These analyses identified elongation factor-1a, ribosomal protein subunit L5 and ribosomal protein subunit 18 as the most stable genes to analyse gene expression during the insect life stages irrespective of Lso presence; Lso haplotype B only affected their respective ranking. By contrast, a common set of normalizers could not be found amongst the different female organs tested (bacteriomes, alimentary canals and reproductive organs).
引用
收藏
页码:227 / 238
页数:12
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