REGULATION OF 5 TUBULIN ISOTYPES BY THYROID-HORMONE DURING BRAIN-DEVELOPMENT

被引:32
作者
ANIELLO, F
COUCHIE, D
GRIPOIS, D
NUNEZ, J
机构
[1] HOP HENRI MONDOR, CNRS, INSERM, U282, F-94010 CRETEIL, FRANCE
[2] UNIV PARIS 11, ENDOCRINOL LAB, F-91405 ORSAY, FRANCE
关键词
TUBULIN; ISOTYPES; THYROID HORMONE; BRAIN DEVELOPMENT;
D O I
10.1111/j.1471-4159.1991.tb06381.x
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
Nucleic acid probes derived from the 3' noncoding region of five tubulin cDNAs were used to study the effects of thyroid hormone deficiency on the expression of the mRNAs encoding two alpha (alpha-1 and alpha-2)- and three beta (beta-2, beta-4, and beta-5)-tubulin isotypes in the developing cerebral hemispheres and cerebellum. The content of alpha-1, which markedly declines during development in both brain regions, is maintained at high levels in the hypothyroid cerebellum, whereas it is decreased in the cerebral hemispheres. The alpha-2 level also declines during development and is decreased in both regions by thyroid hormone deficiency, but only during the two first postnatal weeks. Thyroid hormone deficiency slightly increases at all stages the beta-2 level in the cerebellum, whereas a decrease is observed at early stages in the cerebral hemispheres. The beta-5 level seems to be independent of thyroid hormone in the cerebral hemispheres, whereas it decreases at early stages in the hypothyroid cerebellum. Finally, the expression of the brain-specific beta-4 isotype is markedly depressed by thyroid hormone deficiency, particularly in the cerebellum. These data suggest that the genes encoding the tubulin isotypes are, directly or not, differently regulated by thyroid hormone during brain development. This might contribute to abnormal neurite outgrowth seen in the hypothyroid brain and therefore to impairment in brain functions produced by thyroid hormone deficiency.
引用
收藏
页码:1781 / 1786
页数:6
相关论文
共 45 条
[1]   SPLICING OF JUVENILE AND ADULT TAU-MESSENGER RNA VARIANTS IS REGULATED BY THYROID-HORMONE [J].
ANIELLO, F ;
COUCHIE, D ;
BRIDOUX, AM ;
GRIPOIS, D ;
NUNEZ, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :4035-4039
[2]  
BINDER LI, 1985, J CELL BIOL, V101, P1371, DOI 10.1083/jcb.101.4.1371
[3]   A CHICKEN-YEAST CHIMERIC BETA-TUBULIN PROTEIN IS INCORPORATED INTO MOUSE MICROTUBULES INVIVO [J].
BOND, JF ;
FRIDOVICHKEIL, JL ;
PILLUS, L ;
MULLIGAN, RC ;
SOLOMON, F .
CELL, 1986, 44 (03) :461-468
[4]   FACTORS INFLUENCING POTENTIALS IN NORMAL + CRETINOUS RATS [J].
BRADLEY, PB ;
RICHARDS, NM ;
EAYRS, JT .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1964, 17 (03) :308-+
[5]   BOTH ADULT AND JUVENILE TAU MICROTUBULE-ASSOCIATED PROTEINS ARE AXON SPECIFIC IN THE DEVELOPING AND ADULT-RAT CEREBELLUM [J].
BRION, JP ;
GUILLEMINOT, J ;
COUCHIE, D ;
FLAMENTDURAND, J ;
NUNEZ, J .
NEUROSCIENCE, 1988, 25 (01) :139-146
[6]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[7]   THE MULTITUBULIN HYPOTHESIS REVISITED - WHAT HAVE WE LEARNED [J].
CLEVELAND, DW .
JOURNAL OF CELL BIOLOGY, 1987, 104 (03) :381-383
[8]   EXPRESSION OF THE MESSENGER-RNA FOR TAU-PROTEINS DURING BRAIN-DEVELOPMENT AND IN CULTURED NEURONS AND ASTROGLIAL CELLS [J].
COUCHIE, D ;
CHARRIEREBERTRAND, C ;
NUNEZ, J .
JOURNAL OF NEUROCHEMISTRY, 1988, 50 (06) :1894-1899
[9]   IMMUNOLOGICAL CHARACTERIZATION OF MICROTUBULE-ASSOCIATED PROTEINS SPECIFIC FOR THE IMMATURE BRAIN [J].
COUCHIE, D ;
NUNEZ, J .
FEBS LETTERS, 1985, 188 (02) :331-335
[10]  
CUMMING R, 1983, EUR J CELL BIOL, V31, P241