Differential Expression of Restorer Gene on Different Nuclear Background with Maldandi cytoplasm in Sorghum (Sorghum bicolor (L.) Moench)

Pavan Kumar N, B. D. Biradar, N. G. Hanamaratti, Nethra P, P. Kariyannanavar, .. Revannasiddayya, Prajwal R S
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Abstract

To investigate the expression of restorer gene on different nuclear background an experiment was carried out using six iso-plasmic male sterile lines with maldandi cytoplasm, and each having different nuclear background. These lines were hybridized with a strong and stable restorer to generate six iso-plasmic hybrids at Main Agricultural Research Station (MARS), UAS Dharwad during rabi -2020-21. These hybrids were then evaluated for pollen fertility and seed set percentage during rabi -2021-22. The results found that, pollen fertility percentage of six iso-plasmic hybrids ranged from 69.82 per cent for ICSA 88004 A4 (M) × DSMR 8 to 92.42 per cent for M31-2A (M) × DSMR 8. Similarly, for seed set percentage M31-2A (M) × DSMR 8 and ICSA 88004 A4 (M) × DSMR 8 exhibited highest (85.17 per cent) and lowest (61.19 per cent), respectively. All the six iso-plasmic hybrids had varied expression for pollen fertility and seed set percentage which suggests that the restorer gene expressed differentially in different nuclear genome of female parent. The probable reasons for variation in fertility restoration behaviour are, abundance of inhibitors in the female parent or variation in the expressivity of restorer gene or influence of minor or modifier genes in the restorer parent or interaction between nuclear genes of both the parents.
恢复基因在高粱(Sorghum bicolor (L.) Moench)不同核背景与 Maldandi 细胞质上的差异表达
为了研究还原剂基因在不同核背景下的表达情况,我们使用六个具有雄性不育细胞质的同质雄性不育系进行了实验,每个系都有不同的核背景。在 2020-21 年雨季期间,这些品系与一个强而稳定的恢复基因杂交,在达瓦德大学主要农业研究站(MARS)产生了六个同质杂交种。这些杂交种随后在 2021-22 旱季进行了花粉育性和结实率评估。结果发现,六种同质杂交种的花粉育性百分比从 ICSA 88004 A4 (M) × DSMR 8 的 69.82% 到 M31-2A (M) × DSMR 8 的 92.42% 不等。 同样,在结实率方面,M31-2A (M) × DSMR 8 和 ICSA 88004 A4 (M) × DSMR 8 分别表现出最高(85.17%)和最低(61.19%)。六种同质杂交种的花粉育性和结实率都有不同的表达,这表明育性恢复基因在雌性亲本的不同核基因组中有不同的表达。导致育性恢复行为差异的可能原因是:雌性亲本中存在大量抑制剂,或恢复基因的表达能力存在差异,或恢复基因受亲本中次要基因或修饰基因的影响,或亲本核基因之间存在相互作用。
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