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玉米 T 细胞质中转录体 T-urf13/orf221 的核控制的遗传分析。

Genetic analysis of nuclear control of T-urf13/orf221 transcription in T cytoplasm maize.

机构信息

USDA-ARS, USA.

出版信息

Theor Appl Genet. 1992 Sep;84(7-8):891-8. doi: 10.1007/BF00227401.

Abstract

The mitochondrial gene T-urf13 in T cytoplasm maize is associated with sensitivity to disease toxins and with cytoplasmic male sterility. T-urf13 is co-transcribed with an open reading frame designated orf221. We have detected alterations in the transcription of the T-urf13/orf221 region that are affected by nuclear genotype. There are multiple mRNA transcripts generated from the T-urf13/orf221 region, one of which is a processed 1538-nucleotide (nt) transcript. This 1538-nt transcript is present in Wf9 (T), but was not found in mitochondrial RNAs (mtRNAs) from maize inbreds B14A (T) and 33-16 (T). For B14A (T) a 1500-nt transcript was detected and for 33-16 (T) a 1400-nt transcript was detected. In F1 progeny of the cross of Wf9 (T) x 33-16 (N), only the 1400-nt transcript was present. Genetic analyses revealed this processing event is nuclear controlled with dominant gene action and is independent of nuclear restorer gene Rf1-associated processing events. T-urf13/orf221 transcriptional patterns were shown to vary in both sterile and fertile states. Segregation analysis of a 1100-nt orf221-specific transcript indicated that the genetic basis of nuclear control for the presence of this transcript was relatively simple. Analysis of the A188 (T4) tissue culture mutant, which has reverted to male fertility but displays the same T-urf13/orf221 transcript pattern as A188 (T), indicated no DNA sequence differences between T4-orf221 and T-orf221. Presence of the nuclear gene Rf2 was not necessary for expression of the T4 cytoplasm-associated malefertile phenotype.

摘要

线粒体基因 T-urf13 在 T 细胞质玉米中与疾病毒素的敏感性和细胞质雄性不育有关。T-urf13 与一个开放阅读框 orf221 共同转录。我们已经检测到 T-urf13/orf221 区域的转录变化,这些变化受核基因型的影响。从 T-urf13/orf221 区域产生了多个 mRNA 转录本,其中之一是经过加工的 1538 个核苷酸 (nt) 转录本。这个 1538-nt 转录本存在于 Wf9(T)中,但在玉米自交系 B14A(T)和 33-16(T)的线粒体 RNA(mtRNA)中没有发现。对于 B14A(T),检测到 1500-nt 转录本,对于 33-16(T),检测到 1400-nt 转录本。在 Wf9(T)x33-16(N)杂交的 F1 后代中,只有 1400-nt 转录本存在。遗传分析表明,这种加工事件是由核控制的,具有显性基因作用,并且独立于核恢复基因 Rf1 相关的加工事件。T-urf13/orf221 的转录模式在不育和可育状态下都有所不同。对 1100-nt orf221 特异性转录本的分离分析表明,该转录本的核控制的遗传基础相对简单。对已恢复雄性育性但表现出与 A188(T)相同的 T-urf13/orf221 转录模式的 A188(T4)组织培养突变体的分析表明,T4-orf221 和 T-orf221 之间没有 DNA 序列差异。核基因 Rf2 的存在对于表达 T4 细胞质相关的雄性可育表型不是必需的。

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