The transmission rate of n ＋ 1 gamete is an important parameter for the genetic analysis of trisomics. To correctly use the trisomics of the cabbage to carry out gene orientation and other genetic studies, the n ＋ 1...The transmission rate of n ＋ 1 gamete is an important parameter for the genetic analysis of trisomics. To correctly use the trisomics of the cabbage to carry out gene orientation and other genetic studies, the n ＋ 1 gamete transmission rates by female parent and by male parent were determined. The results showed that the n ＋ 1 gamete transmission rates were 15.28% for tri-1, 12.68% for tri-2, 12.31% for tri-3, 30.51% for tri-4, 22.81% for tri-5, 7.46% for tri-6, 5.36% for tri-7, 42.37% for tri-8, and 9.23% for tri-9 by female parent, and were 12.12% for tri-1, 12.33% for tri-2, 7.81% for tri-3, 4.76% for tri-4, 8.93% for tri-5, 10.94% for tri-6, 1.54% for tri-7, 2.94% for tri-8, and 13.04% for tri-9 by male parent. The main factors affecting the male n ＋ 1 gamete formation and transmission were the rate of trivalent formation at prophase Ⅰ, the rate of 9-9-10-10 division at anaphase Ⅱ, and the pollen viability.展开更多
Both female and male gametophytes harbor companion cells and gametes. MET1, a DNA methyltransferase, is down-regulated in companion cells. However, how MET1 is differentially regulated in gametophytes remains unexplor...Both female and male gametophytes harbor companion cells and gametes. MET1, a DNA methyltransferase, is down-regulated in companion cells. However, how MET1 is differentially regulated in gametophytes remains unexplored. ARID1, a transcription factor that is specifically depleted in sperm cells, is occupied by MET1- dependent CG methylation. Here, we show that MET1 confines ARID1 to the vegetative cell of male gametes, but ARID1 conversely represses MET1 in the central cell of female gametes. Compared to the vegetative celllocalization in wild type pollen, ARID1 expands to sperm cells in the met1 mutant. To understand whether MET1- dependent ARID1 inhibition exists during female gametogenesis, we first show that ARID1 is expressed in the megaspore mother cell （MMC）, ARID1 but not MET1 is detectable in the central cell at maturity. Interestingly, compared to the absence of MET1 in the central cell and the egg cell of wild type ovules, MET1 significantly accumulates in these two cells in aridl ovules. Lastly, we show that both ARIDI and METI are required for the cell specification of MMC. Collectively, our results uncover a reciprocal dependence between ARIDI and METI, and provide a clue to further understand how the specification of MMC is likely regulated by DNA methylation.展开更多
基金the Natural Science Foundation of Hebei Province, China （C2006000450）.
文摘The transmission rate of n ＋ 1 gamete is an important parameter for the genetic analysis of trisomics. To correctly use the trisomics of the cabbage to carry out gene orientation and other genetic studies, the n ＋ 1 gamete transmission rates by female parent and by male parent were determined. The results showed that the n ＋ 1 gamete transmission rates were 15.28% for tri-1, 12.68% for tri-2, 12.31% for tri-3, 30.51% for tri-4, 22.81% for tri-5, 7.46% for tri-6, 5.36% for tri-7, 42.37% for tri-8, and 9.23% for tri-9 by female parent, and were 12.12% for tri-1, 12.33% for tri-2, 7.81% for tri-3, 4.76% for tri-4, 8.93% for tri-5, 10.94% for tri-6, 1.54% for tri-7, 2.94% for tri-8, and 13.04% for tri-9 by male parent. The main factors affecting the male n ＋ 1 gamete formation and transmission were the rate of trivalent formation at prophase Ⅰ, the rate of 9-9-10-10 division at anaphase Ⅱ, and the pollen viability.
基金supported by grants of the National Natural Science Foundation of China(31422029,31470281,31671261)the Recruitment Program of Global Experts(China)
文摘Both female and male gametophytes harbor companion cells and gametes. MET1, a DNA methyltransferase, is down-regulated in companion cells. However, how MET1 is differentially regulated in gametophytes remains unexplored. ARID1, a transcription factor that is specifically depleted in sperm cells, is occupied by MET1- dependent CG methylation. Here, we show that MET1 confines ARID1 to the vegetative cell of male gametes, but ARID1 conversely represses MET1 in the central cell of female gametes. Compared to the vegetative celllocalization in wild type pollen, ARID1 expands to sperm cells in the met1 mutant. To understand whether MET1- dependent ARID1 inhibition exists during female gametogenesis, we first show that ARID1 is expressed in the megaspore mother cell （MMC）, ARID1 but not MET1 is detectable in the central cell at maturity. Interestingly, compared to the absence of MET1 in the central cell and the egg cell of wild type ovules, MET1 significantly accumulates in these two cells in aridl ovules. Lastly, we show that both ARIDI and METI are required for the cell specification of MMC. Collectively, our results uncover a reciprocal dependence between ARIDI and METI, and provide a clue to further understand how the specification of MMC is likely regulated by DNA methylation.
