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Authors
Advisor(s)
Abstract(s)
A quantitative PCR (Q-PCR) method has been established to measure
the mRNA expression levels of parathyroid hormone–related protein
(PTHrP), parathyroid hormone receptor type 1 (PTHR1), and calcium-sensing
receptor (CaSR) in sea bream (Sparus aurata), using the housekeeping gene, -
actin, as endogenous control. TaqMan primers and probes were designed using
the Primer Express program, according to the published/unpublished sequences
of the three target genes and -actin of sea bream. Different tissues including
gill, kidney, duodenum, hindgut, rectum, liver, heart, brain, pituitary, skin,
muscle, and gonad were removed and immediately snap-frozen from three
juvenile sea bream (100–150 g) cultured in sea water. The mRNAs were extracted
and reverse-transcribed into cDNAs, which were subsequently examined
by the ABI 5700 system using an optimized Q-PCR method. Triplicate measures
of each sample indicated consistency of the technique. However, the mRNA
expression levels for each transcript in these tissues were variable between fish
and also relatively low. Nevertheless, this methodology can be used in the future
studies of factors that may alter gene expression in these tissues.
Description
Keywords
Q-PCR PTHrP PTHRP1 CaSR Sea bream
Citation
Hang XM, Power D, Flik G, Balment RJ., "Measurement of PTHrP, PTHR1, and CaSR expression levels in tissues of sea bream (Sparus aurata) using quantitative PCR" in Ann N Y Acad Sci. 2005 Apr;1040:340-4.
Publisher
Wiley