Identification of an asymmetrically localized determinant, Ash1p, required for lineage-specific transcription of the yeast HO gene

被引:215
|
作者
Sil, A
Herskowitz, I
机构
[1] Dept. of Biochemistry and Biophysics, Univ. of California, San Francisco, San Francisco
关键词
D O I
10.1016/S0092-8674(00)81049-1
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
S. cerevisiae cells exhibit asymmetric determination of cell fate. Cell division yields a mother cell, which is competent to transcribe the HO gene and switch mating type, and a daughter cell, which is not. We have isolated a mutant in which daughters transcribe HO and switch mating type. This mutation defines the ASH1 gene (asymmetric synthesis of HO). Deletion and overexpression of ASH1 cause reciprocal cell fate transformations: in ash1 Delta strains, daughters switch mating type as efficiently as mothers. Conversely, overexpression of ASH1 inhibits switching in mother cells. Ash1p has a zinc finger motif related to those of GATA transcriptional regulators. Ash1p is localized to the daughter nucleus in cells that have undergone nuclear division. Thus, Ash1p is a cell fate determinant that is asymmetrically localized to the daughter nucleus where it inhibits HO transcription.
引用
收藏
页码:711 / 722
页数:12
相关论文
共 18 条
  • [1] Efficient mRNA localization and translational control are required for Ash1p sorting in yeast
    Chartrand, P
    Meng, X
    Huettelmaier, S
    Donato, D
    Singer, RH
    MOLECULAR BIOLOGY OF THE CELL, 2002, 13 : 522A - 523A
  • [2] Ash1p is a site-specific DNA-binding protein that actively represses transcription
    Maxon, ME
    Herskowitz, I
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (04) : 1495 - 1500
  • [3] The Ames dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage-specific cell proliferation
    Gage, PJ
    Brinkmeier, ML
    Scarlett, LM
    Knapp, LT
    Camper, SA
    Mahon, KA
    MOLECULAR ENDOCRINOLOGY, 1996, 10 (12) : 1570 - 1581
  • [4] Homeodomain proteins MEIS1 and PBXs regulate the lineage-specific transcription of the platelet factor 4 gene
    Okada, Y
    Nagai, R
    Sato, T
    Matsuura, E
    Minami, T
    Morita, I
    Doi, T
    BLOOD, 2003, 101 (12) : 4748 - 4756
  • [5] Exogenous TPRX1 homeoprotein modulates the gene expression of lineage-specific transcription factors in human embryonal carcinoma cells
    Mori, Yuki
    Sakuraoka, Mizuki
    Suzuki, Takahiro
    Sato, Sho
    Sugawara, Saiko
    Hiraide, Misuzu
    Sato, Suguru
    Kobayashi, Masayuki
    BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT, 2018, 32 (03) : 646 - 652
  • [6] A lineage-specific arginine in POS1 is required for fruit size control in Physaleae (Solanaceae) via gene co-option
    Wang, Li
    Liu, Xueyang
    Li, Qiaoru
    Xu, Nan
    He, Chaoying
    PLANT JOURNAL, 2022, 111 (01): : 183 - 204
  • [7] Identification of a pituitary ERα-activated enhancer triggering the expression of Nr5a1, the earliest gonadotrope lineage-specific transcription factor
    Vincent Pacini
    Florence Petit
    Bruno Querat
    Jean-Noël Laverriere
    Joëlle Cohen-Tannoudji
    David L’hôte
    Epigenetics & Chromatin, 12
  • [8] Identification of a pituitary ERα-activated enhancer triggering the expression of Nr5a1, the earliest gonadotrope lineage-specific transcription factor
    Pacini, Vincent
    Petit, Florence
    Querat, Bruno
    Laverriere, Jean-Noel
    Cohen-Tannoudji, Joelle
    L'hote, David
    EPIGENETICS & CHROMATIN, 2019, 12 (01)
  • [9] Transcription factor B cell lineage-specific activator protein regulates the gene for human X-box binding protein 1
    Reimold, AM
    Ponath, PD
    Li, YS
    Hardy, RR
    David, CS
    Strominger, JL
    Glimcher, LH
    JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (02): : 393 - 401
  • [10] Identification of a polymorphic gene, BCL2A1, encoding two novel hematopoietic lineage-specific minor histocompatibility antigens
    Akatsuka, Y
    Nishida, T
    Kondo, E
    Miyazaki, M
    Taji, H
    Iida, H
    Tsujimura, K
    Yazaki, M
    Naoe, T
    Morishima, Y
    Kodera, Y
    Kuzushima, K
    Takahashi, T
    JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (11): : 1489 - 1500