TY - JOUR
T1 - Mining microarrays for metabolic meaning
T2 - Nutritional regulation of hypothalamic gene expression
AU - Mobbs, Charles V.
AU - Yen, Kelvin
AU - Mastaitis, Jason
AU - Nguyen, Ha
AU - Watson, Elizabeth
AU - Wurmbach, Elisa
AU - Sealfon, Stuart C.
AU - Brooks, Andrew
AU - Salton, Stephen R.J.
N1 - Funding Information:
Preparation of this manuscript and work in the authors’ laboratories was supported by grants NIH NS45305, NIH DK57702, AHA350085N (S. R. J. S.); NIH NS41183-01, NIH AG19934-01, and the Juvenile Diabetes Research Foundation (C. V. M.); and NIH DK46943 (S. C. S.). Elizabeth Watson was supported by NIH Endocrine Training Grant 5T32DK07645.
PY - 2004/6
Y1 - 2004/6
N2 - DNA microarray analysis has been used to investigate relative changes in the level of gene expression in the CNS, including changes that are associated with disease, injury, psychiatric disorders, drug exposure or withdrawal, and memory formation. We have used oligonucleotide microarrays to identify hypothalamic genes that respond to nutritional manipulation. In addition to commonly used microarray analysis based on criteria such as fold-regulation, we have also found that simply carrying out multiple t tests then sorting by P value constitutes a highly reliable method to detect true regulation, as assessed by real-time polymerase chain reaction (PCR), even for relatively low abundance genes or relatively low magnitude of regulation. Such analyses directly suggested novel mechanisms that mediate effects of nutritional state on neuroendocrine function and are being used to identify regulated gene products that may elucidate the metabolic pathology of obese ob/ob, lean Vgf-/Vgf-, and other models with profound metabolic impairments.
AB - DNA microarray analysis has been used to investigate relative changes in the level of gene expression in the CNS, including changes that are associated with disease, injury, psychiatric disorders, drug exposure or withdrawal, and memory formation. We have used oligonucleotide microarrays to identify hypothalamic genes that respond to nutritional manipulation. In addition to commonly used microarray analysis based on criteria such as fold-regulation, we have also found that simply carrying out multiple t tests then sorting by P value constitutes a highly reliable method to detect true regulation, as assessed by real-time polymerase chain reaction (PCR), even for relatively low abundance genes or relatively low magnitude of regulation. Such analyses directly suggested novel mechanisms that mediate effects of nutritional state on neuroendocrine function and are being used to identify regulated gene products that may elucidate the metabolic pathology of obese ob/ob, lean Vgf-/Vgf-, and other models with profound metabolic impairments.
KW - Brain
KW - Diabetes
KW - Fasting
KW - Hypothalamus
KW - Microarray
KW - Obesity
UR - https://www.scopus.com/pages/publications/3142724651
U2 - 10.1023/B:NERE.0000023596.49140.e0
DO - 10.1023/B:NERE.0000023596.49140.e0
M3 - Review article
C2 - 15176466
AN - SCOPUS:3142724651
SN - 0364-3190
VL - 29
SP - 1093
EP - 1103
JO - Neurochemical Research
JF - Neurochemical Research
IS - 6
ER -