CENP-F is a protein of the nuclear matrix that assembles onto kinetochores at late G2 and is rapidly degraded after mitosis.
CENP-F is a protein of the nuclear matrix that assembles onto kinetochores at late G2 and is rapidly degraded after mitosis.
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CENP-F是一种核基质的蛋白质,该核基质在G2晚期聚集在动力学上,并在有丝分裂后迅速降解。
DOI:
10.1083/jcb.130.3.507
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发表时间:
1995-08
影响因子:
7.8
通讯作者:
YEN, TJ
中科院分区:
文献类型:
--
作者:
LIAO, H;WINKFEIN, RJ;MACK, G;RATTNER, JB;YEN, TJ
Centromere protein-F (CENP-F) is mammalian kinetochore protein that was recently identified by an autoimmune serum (Rattner, J. B., A. Rao, M. J. Fritzler, D. W. Valencia, and T. J. Yen. Cell Motil. Cytoskeleton. 26:214-226). We report here the human cDNA sequence of CENP-F, along with its expression and localization patterns at different stages of the HeLa cell cycle. CENP-F is protein of the nuclear matrix that gradually accumulates during the cell cycle until it reaches peak levels in G2 and M phase cells and is rapidly degraded upon completion of mitosis. CENP-F is first detected at the prekinetochore complex during late G2, and is clearly detectable as paired foci that correspond to all the centromeres by prophase. During mitosis, CENP-F is associated with kinetochores from prometaphase until early anaphase and is then detected at the spindle midzone throughout the remainder of anaphase. By telophase, CENP-F is concentrated within the intracellular bridge at either side of the mid-body. The predicted structure of the 367-kD CENP-F protein consists of two 1,600-amino acid-long coil domains that flank a central flexible core. A putative P-loop nucleotide binding site (ADIPTGKT) is located within the globular carboxy terminus. The structural features deduced from our sequence studies and the spatial and temperal distribution of CENP-F revealed in our cytological and biochemical studies suggest that it may play a role in several mitotic events.
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影响因子:
7.8
作者:
GOH, PY;KILMARTIN, JV
通讯作者:
KILMARTIN, JV
DOI:
10.1073/pnas.83.4.907
发表时间:
1986-02-01
影响因子:
11.1
作者:
FRY, DC;KUBY, SA;MILDVAN, AS
通讯作者:
MILDVAN, AS
影响因子:
64.8
作者:
HYMAN, AA;MIDDLETON, K;CARBON, J
通讯作者:
CARBON, J
DOI:
10.1083/jcb.127.2.303
发表时间:
1994-10
期刊:
The Journal of cell biology
影响因子:
--
作者:
Saitoh N;Goldberg IG;Wood ER;Earnshaw WC
通讯作者:
Earnshaw WC
DOI:
10.1073/pnas.91.15.7212
发表时间:
1994-07-19
影响因子:
11.1
作者:
MIDDLETON, K;CARBON, J
通讯作者:
CARBON, J