Li Long, Cui Shunli, Li Xiukun, Hou Mingyu, Liu Yingru, Liu Lifeng
College of Agronomy, State Key Laboratory of North China for Crop Improvement and Regulation/Key laboratory of Crop Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, 071001, P.R. China.
BMC Genomics. 2025 Apr 15;26(1):376. doi: 10.1186/s12864-025-11560-7.
Peanut (Arachis hypogaea L., 2n = 2x = 20) is an important industrial and oil crop that is widely grown in more than 100 countries. In recent years, breeders have focused on increasing the seed number per pod to improve their yield in addition to other breeding for other key components of yield, including the pod number, seeds per pod, and 100-seed weight.
In this study, a secondary population of 1,114 BCF lines was derived from a cross between the parents R45 and JNH3. Two stable major-effect quantitative trait loci of qRMPA09.1 and qRMPA09.2 were detected simultaneously and mapped within chromosomal intervals of approximately 400 Kb and 600 Kb on chromosome A09. Additionally, combined whole-genome and RNA sequencing analyses showed the differential expression of the Arahy.04JNDX gene that belongs to a MYB transcription factor (TF) between the two parents. The AhMYB51 gene was also inferred to influence the number of seeds per pod in peanuts. An examination of the backcross lines L/L showed that AhMYB51 increases the rate of multiple pods per plant (RMSP) primarily by affecting brassinosteroids in the flowers, while its overexpression promotes the length of siliques in Arabidopsis thaliana.
Our findings provide valuable insights for the cloning of favorable alleles for RMSP in peanuts. The qRMSPA09.1 and qRMSPA09.2 are two novel QTL associated with the RMSP trait, with AhMYB51 predicted as its candidate gene. Moreover, the closely linked polymorphic SNP markers for loci of two significant QTLs may be useful in accelerating marker-assisted breeding in peanuts.
花生(Arachis hypogaea L.,2n = 2x = 20)是一种重要的工业和油料作物,在100多个国家广泛种植。近年来,除了对产量的其他关键组成部分(包括荚果数、每荚种子数和百粒重)进行育种外,育种者还专注于增加每荚种子数以提高产量。
在本研究中,从亲本R45和JNH3的杂交中获得了1114个BCF株系的次级群体。同时检测到两个稳定的主效数量性状位点qRMPA09.1和qRMPA09.2,并将其定位在A09染色体上约400 Kb和600 Kb的染色体区间内。此外,全基因组和RNA测序联合分析显示,两个亲本之间属于MYB转录因子(TF)的Arahy.04JNDX基因存在差异表达。还推断AhMYB51基因影响花生的每荚种子数。对回交株系L/L的检测表明,AhMYB51主要通过影响花中的油菜素类固醇来提高单株多荚率(RMSP),而其过表达促进拟南芥角果的长度。
我们的研究结果为花生RMSP有利等位基因的克隆提供了有价值的见解。qRMSPA09.1和qRMSPA09.2是与RMSP性状相关的两个新的QTL,预测AhMYB51为其候选基因。此外,两个重要QTL位点紧密连锁的多态性SNP标记可能有助于加速花生的分子标记辅助育种。