首页> 美国卫生研究院文献>Horticulture Research >SCR-22 of pollen-dominant S haplotype class is recessive to SCR-44 of pollen-recessive S haplotype class in Brassica rapa
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SCR-22 of pollen-dominant S haplotype class is recessive to SCR-44 of pollen-recessive S haplotype class in Brassica rapa

机译:花粉显性S单倍型类别的SCR-22相对于甘蓝型油菜隐性S单倍型类别的SCR-44是隐性的

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摘要

SCR/SP11 encodes the male determinant of recognition specificity of self-incompatibility (SI) in Brassica species and is sporophytically expressed in the anther tapetum. Based on dominance relationships in pollen and nucleotide sequence similarity, the S haplotypes in Brassica have been classified as class I or class II, with class-I S haplotypes being dominant over class-II S haplotypes. Here, we revealed that S-22 in B. rapa belonging to class I is recessive to class-II S-44 and class-I S-36 in pollen, whereas it is dominant over S-60, S-40, and S-29 based on pollination tests. SCR/SP11 of S-22 (SCR-22) was sequenced, revealing that the deduced amino-acid sequence of SCR-22 has the longest C-terminal domain among the SCR/SP11 sequences. The expression of SCR-22 was found to be suppressed in S-22/S-44 and S-22/S-36 heterozygotes. Normal transcription of SCR-44 was considered to be due to the transcription suppression of Smi sRNA of the S-22 haplotype and a very low methylation state of the SCR-44 promoter region in the tapetum of S-22/S-44 heterozygotes. In SCR-22, only the cytosine residue located at the –37 bp position of the promoter region was hypermethylated in the tapetum of S-22/S-44 heterozygotes, and few methylated cytosines were detected in the promoter and coding regions of SCR-22 in S-22/S-36 heterozygotes. SCR-22 was also expressed in microspores in S-22 homozygotes but not in S-22/S-44 and S-22/S-36 heterozygotes. These results suggest that a mechanism different from class-II SCR/SP11 suppression may operate for the suppression of recessive class-I SCR-22 in S heterozygotes.
机译:SCR / SP11编码芸苔属物种中自交不亲和性(SI)识别特异性的雄性决定因子,并在花药绒毡层中孢子体表达。基于花粉的优势关系和核苷酸序列相似性,甘蓝型油菜的单倍型已被分类为I类或II类,其中I类S单倍型比II类S单倍型占优势。在这里,我们发现属于I类的B. rapa中的S-22对花粉中的II类S-44和I类S-36是隐性的,而在S-60,S-40和S上占主导地位-29基于授粉测试。对S-22(SCR-22)的SCR / SP11进行了测序,揭示了SCR-22推导的氨基酸序列在SCR / SP11序列中具有最长的C末端结构域。发现 SCR-22 的表达在 S-22 / S-44 S-22 / S-36 杂合子中被抑制。认为 SCR-44 的正常转录是由于 S-22 单倍型的 Smi sRNA的转录抑制和极低的甲基化S-22 / S-44 杂合子绒毡层中 SCR-44 启动子区域的状态。在 SCR-22 中,只有位于启动子区域–37 bp位置的胞嘧啶残基在 S-22 / S-44 杂合子的绒毡层中被高度甲基化,而在 S-22 / S-36 杂合子的 SCR-22 的启动子和编码区中检测到很少的甲基化胞嘧啶。 SCR-22 S-22 纯合子中也表达于小孢子中,但在 S-22 / S-44 S- 22 / S-36 杂合子。这些结果表明,不同于II类 SCR / SP11 抑制的机制可能对抑制隐性I类 SCR-22 起作用。 S 杂合子。

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