Gene expression analysis of the function of the male-specific lethal complex in drosophila

被引:44
|
作者
Bhadra, MP
Bhadra, U
Kundu, J
Birchler, JA
机构
[1] Univ Missouri, Div Biol Sci, Columbia, MO 65211 USA
[2] Ctr Cellular & Mol Biol, Funct Genom & Gene Silencing Grp, Hyderabad 500007, Andhra Pradesh, India
关键词
D O I
10.1534/genetics.104.036020
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Dosage compensation refers to the equal expression of X-linked genes despite the difference in copy number between the two sexes. The mate-specific lethal (MSL) complex is concentrated on the X chromosome in males. A gene expression assay for embryos was developed to examine the function of this complex. In mutant male embryos without either the MSL complex or MOF historic acetylase, dosage compensation is retained but autosomal expression is increased. Dosage compensation is lost in the double-mutant embryos. In embryos in which the MSL complex and MOF are targeted to the X chromosomes in females, the results are consistent with previous surveys showing that in general the X expression remains unchanged, but autosomal expression is reduced. Mutations in the ISWI chromatin-remodeling component cause increases specifically of X-linked genes in males. Thus, the function of the MSL complex in conjunction with ISWI is postulated to override the effect on gene expression of high histone acetylation on the male X. The basic determinant of dosage compensation is suggested to be an inverse dosage effect produced by an imbalance of transcription factors on the X vs. the autosomes. The sequestration of the MSL complex to the male X may have evolved to counteract a similar effect on the autosomes and to prevent an overexpression of the X chromosome in males that would otherwise occur due to the high levels of histone acetylation.
引用
收藏
页码:2061 / 2074
页数:14
相关论文
共 50 条
  • [31] The Drosophila roX1 RNA gene can overcome silent chromatin by recruiting the male-specific lethal dosage compensation complex
    Kelley, RL
    Kuroda, MI
    GENETICS, 2003, 164 (02) : 565 - 574
  • [32] Drosophila male-specific lethal-2 protein: Structure/function analysis and dependence on MSL-1 for chromosome association
    Lyman, LM
    Copps, K
    Rastelli, L
    Kelley, RL
    Kuroda, MI
    GENETICS, 1997, 147 (04) : 1743 - 1753
  • [33] Sequence signatures involved in targeting the male-specific lethal complex to X-chromosomal genes in Drosophila melanogaster
    Philge Philip
    Fredrik Pettersson
    Per Stenberg
    BMC Genomics, 13
  • [34] Proximity ligation assays of protein and RNA interactions in the male-specific lethal complex on Drosophila melanogaster polytene chromosomes
    Lindehell, Henrik
    Kim, Maria
    Larsson, Jan
    CHROMOSOMA, 2015, 124 (03) : 385 - 395
  • [35] Sequence signatures involved in targeting the male-specific lethal complex to X-chromosomal genes in Drosophila melanogaster
    Philip, Philge
    Pettersson, Fredrik
    Stenberg, Per
    BMC GENOMICS, 2012, 13
  • [36] Conservation of male-specific expression of novel phosphoprotein phosphatases in Drosophila
    Csaba Ádám
    László Henn
    Márton Miskei
    Miklós Erdélyi
    Péter Friedrich
    Viktor Dombrádi
    Development Genes and Evolution, 2010, 220 : 123 - 128
  • [37] Proximity ligation assays of protein and RNA interactions in the male-specific lethal complex on Drosophila melanogaster polytene chromosomes
    Henrik Lindehell
    Maria Kim
    Jan Larsson
    Chromosoma, 2015, 124 : 385 - 395
  • [38] Conservation of male-specific expression of novel phosphoprotein phosphatases in Drosophila
    Adam, Csaba
    Henn, Laszlo
    Miskei, Marton
    Erdelyi, Miklos
    Friedrich, Peter
    Dombradi, Viktor
    DEVELOPMENT GENES AND EVOLUTION, 2010, 220 (3-4) : 123 - 128
  • [40] Origin and evolution of the regulatory gene male-specific lethal-3
    Marín, I
    Baker, BS
    MOLECULAR BIOLOGY AND EVOLUTION, 2000, 17 (08) : 1240 - 1250