Munguambe Nilsa Emilia, Inoue Shouta, Demeter Zita, Yamagata Yoshiyuki, Yasui Hideshi, Zheng Shao-Hui, Fujita Daisuke
Tropical Crop Improvement Laboratory, Faculty of Agriculture, Saga University, Saga, Japan.
Plant Breeding Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka, Japan.
Front Plant Sci. 2021 Apr 21;12:633247. doi: 10.3389/fpls.2021.633247. eCollection 2021.
Hybrid breakdown, a form of postzygotic reproductive barrier, has been reported to hinder gene flow in many crosses between wild and cultivated rice. Here, the phenomenon of hybrid breakdown was observed as low-tillering (i.e., low tiller number) in some progeny of an interspecific cross produced in an attempt to introduce Ng (W1625) chromosomal segments into L. ssp. "Taichung 65" (T65). Low-tillering lines were obtained in BC-derived progeny from a cross between W1625 and "Taichung 65," but the locus for low-tillering could not be mapped in segregating populations. As a second approach to map the locus for low-tillering, we analyzed an F population derived from a cross between the low-tillering lines and a high-yielding cultivar, "Takanari." A major QTL for low-tillering, , was detected between PCR-based markers MS10 and RM307 on the long arm of chromosome 4, with a LOD score of 15.6. The low-tillering phenotype was associated with weak growth and pale yellow phenotype; however, low-tillering plant had less reduction of grain fertility. In an F population (4896 plants), 563 recombinant plants were identified and the low-tillering locus was delimited to a 4.6-Mbp region between markers W1 and C5-indel3729. This region could not be further delimited because recombination is restricted in this region of , which is near the centromere. Understanding the genetic basis of hybrid breakdown, including the low-tillering habit, will be important for improving varieties in rice breeding.
杂种衰败是一种合子后生殖障碍形式,据报道在许多野生稻和栽培稻杂交中会阻碍基因流动。在此,在一个种间杂交的一些后代中观察到杂种衰败现象表现为低分蘖(即分蘖数少),该种间杂交旨在将Ng(W1625)染色体片段导入粳稻亚种“台中65”(T65)。在W1625与“台中65”杂交产生的回交后代中获得了低分蘖株系,但在分离群体中无法定位低分蘖位点。作为定位低分蘖位点的第二种方法,我们分析了一个由低分蘖株系与高产栽培品种“越光”杂交产生的F群体。在第4染色体长臂上基于PCR的标记MS10和RM307之间检测到一个控制低分蘖的主效QTL,命名为LT1,其LOD值为15.6。低分蘖表型与生长势弱和浅黄色表型相关;然而,低分蘖植株的籽粒育性降低较少。在一个F群体(4896株)中,鉴定出563株重组植株,并将低分蘖位点限定在标记W1和C5 - indel3729之间4.6兆碱基对的区域。由于在第4染色体这个靠近着丝粒的区域重组受到限制,该区域无法进一步界定。了解杂种衰败的遗传基础,包括低分蘖习性,对于水稻育种中的品种改良将具有重要意义。